JPH0253704A - Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active component - Google Patents
Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active componentInfo
- Publication number
- JPH0253704A JPH0253704A JP63205251A JP20525188A JPH0253704A JP H0253704 A JPH0253704 A JP H0253704A JP 63205251 A JP63205251 A JP 63205251A JP 20525188 A JP20525188 A JP 20525188A JP H0253704 A JPH0253704 A JP H0253704A
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- compound
- insecticidal
- group
- ethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 title abstract description 27
- 230000000749 insecticidal effect Effects 0.000 title abstract description 8
- 230000003129 miticidal effect Effects 0.000 title abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 10
- 239000000642 acaricide Substances 0.000 claims abstract description 6
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- 125000005843 halogen group Chemical group 0.000 claims abstract description 4
- 239000002917 insecticide Substances 0.000 claims description 13
- 230000000895 acaricidal effect Effects 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 3
- 125000001033 ether group Chemical group 0.000 claims 1
- 150000003217 pyrazoles Chemical class 0.000 abstract description 5
- -1 methoxy, ethoxy Chemical group 0.000 abstract description 4
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 abstract description 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 241000238631 Hexapoda Species 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 241001454293 Tetranychus urticae Species 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 241001556089 Nilaparvata lugens Species 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 241000238876 Acari Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241001414720 Cicadellidae Species 0.000 description 2
- 241000258937 Hemiptera Species 0.000 description 2
- 241000238681 Ixodes Species 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 241000500437 Plutella xylostella Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 150000001412 amines Chemical group 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 230000002688 persistence Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 210000003296 saliva Anatomy 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- WRKWQCNJAZPEKK-UHFFFAOYSA-N 5-methyl-1h-pyrazole-3-carboxamide Chemical compound CC=1C=C(C(N)=O)NN=1 WRKWQCNJAZPEKK-UHFFFAOYSA-N 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000256054 Culex <genus> Species 0.000 description 1
- 241000256059 Culex pipiens Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000336797 Eoeurysa flavocapitata Species 0.000 description 1
- 241001466042 Fulgoromorpha Species 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 241000721621 Myzus persicae Species 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000034303 cell budding Effects 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 230000009850 completed effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 231100000194 ovacidal Toxicity 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は新規なピラゾール類およびこれを有効成分とす
る殺虫、殺ダニ剤および動物に寄生するダニの駆除剤に
関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to novel pyrazoles and insecticides, acaricides, and agents for killing mites parasitic on animals that contain the same as an active ingredient.
本発明の化合物と類似の構造を有する化合物のうち、殺
菌活性を有するものがPe5t、 Bio。Among the compounds having a similar structure to the compounds of the present invention, those having bactericidal activity are Pe5t and Bio.
Phy、+ 2!;、 /乙3(/9g&)、特開昭3
2−gqitg号公報および特開昭A O−,74(9
19号公報に、また除草活性を有するものが特開昭!;
7−10AAI、!r号公報に、また医薬活性を有する
ものが特開昭弘7−626?号公報、特開昭11g−!
;41,7/号公報、特開昭32−gJg’IO号公報
、特公昭3S−99757号公報、特開昭5t−7,3
07/号公報、特開昭、!t?−9!;27コ号公報お
よびJ、Pharm、Sci、、 ?i、 10/JC
/ 9g!;)に各々、記載されているが、殺虫、殺ダ
ニ活性についての報告は全くない。また、上記公報およ
び文献中には、アミン部分の置換基として、アラルキル
基については全く記載されていない。Phy, +2! ;, /Otsu 3 (/9g&), Tokukai Sho 3
2-gqitg publication and JP-A-ShoA O-, 74 (9
In Publication No. 19, there is also a substance with herbicidal activity published in JP-A-Sho! ;
7-10AAI,! In Japanese Patent Publication No. R, Akihiro 7-626, which has medicinal activity, Publication No. 11g-!
;41,7/ Publication, Japanese Patent Application Publication No. 32-gJg'IO, Japanese Patent Publication No. 3S-99757, Japanese Patent Application Publication No. 3S-99757, Publication No. 5t-7,3
07/No. Publication, JP-A-Sho,! T? -9! ;27 Publication and J, Pharm, Sci, ? i, 10/JC
/ 9g! ;), but there are no reports on insecticidal or acaricidal activity. Further, in the above-mentioned publications and literatures, there is no mention of an aralkyl group as a substituent for the amine moiety.
一方、Farmaco、 Ed、5ci−e 22.
t 92 (/ 917 )KU、N−ベンジル−3i
メチル−5−ピラゾールカルボキサミドおよび3−メチ
ル−S−ピラゾールカルボン酸ペンジルエステルカ、マ
タ、Rev、Roum、Chim、+ 2.、?+
/ 左ざ/ (/ 97g )には、N−ベンジル−
/−(2,Q−ジニトロフェニルクー3−ビフェニル−
5−ピラゾールカルボキサミドが、まだ特開昭!; 0
− !rl!:0!rA号公報には、N−(Q−ヒドロ
キシベンジル)−/、、?−ジメチルー5−ピラゾール
カルボキサミドおよびN−(クーヒドロキシカルボニル
メトキシベンジル)−i、、y−ジメチル−3−ピラゾ
ールカルボキサミドが記載されているが、該化合物の殺
虫、殺ダニ活性の有無についての報告は全くない。On the other hand, Farmaco, Ed, 5ci-e 22.
t92 (/917) KU, N-benzyl-3i
Methyl-5-pyrazolecarboxamide and 3-methyl-S-pyrazolecarboxylic acid pendyl ester, Rev, Roum, Chim, +2. ,? +
/ Left side / (/97g) contains N-benzyl-
/-(2,Q-dinitrophenyl-3-biphenyl-
5-pyrazole carboxamide is still in Japanese patent publication! ; 0
−! rl! :0! In the rA publication, N-(Q-hydroxybenzyl)-/,? -dimethyl-5-pyrazolecarboxamide and N-(couhydroxycarbonylmethoxybenzyl)-i,,y-dimethyl-3-pyrazolecarboxamide have been described, but there have been no reports on whether or not these compounds have insecticidal or acaricidal activity. do not have.
また、アミン部分がトリアルキルシリルベンジルアミン
であるカルボキサミド類については全く報告されていな
い。Further, there have been no reports on carboxamides in which the amine moiety is trialkylsilylbenzylamine.
近年、殺虫剤の長年の使用により害虫に抵抗性が生じ、
従来の殺虫剤による防除が困難となっている。例えば代
表的殺虫剤である有機リン剤5カーバメート剤に対して
は広く抵抗性害虫が発生し防除が困難となっている。ま
た、近年注目されてきた合成ピレスロイド系殺虫剤に対
しても抵抗性の発達した害虫が報告されている。In recent years, long-term use of insecticides has caused insects to become resistant.
Control using conventional insecticides has become difficult. For example, a wide range of insect pests have become resistant to organophosphorous 5-carbamate agents, which are typical insecticides, making it difficult to control them. In addition, insect pests that have developed resistance to synthetic pyrethroid insecticides, which have attracted attention in recent years, have been reported.
=方、有機リン剤あるいはカーバメート剤のあるものは
毒性が高く、またあるものは残留性により生態系を乱す
ためきわめて憂慮すべき状況となっている。従って、従
来の殺虫剤に抵抗性を示す害虫に対しても優れた防除効
果を示し、しかも低毒性かつ低残留性の新規な殺虫剤の
開発が期待されている。On the other hand, some organic phosphorus agents or carbamate agents are highly toxic, and others disturb the ecosystem due to their persistence, creating an extremely worrying situation. Therefore, the development of new insecticides that exhibit excellent control effects even against insect pests that are resistant to conventional insecticides, and that have low toxicity and low persistence are expected.
本発明者らは、上記問題点に鑑み、鋭意研究を行った結
果、優れた殺虫殺ダニ活性を有する新規なピラゾール誘
導体を見出し、本発明を完成するに至った。In view of the above problems, the present inventors conducted extensive research, and as a result, discovered a novel pyrazole derivative having excellent insecticidal and acaricidal activity, and completed the present invention.
すなわち、本発明の要旨は、下記一般式CI)で表され
るピラゾール類およびこれを有効成分として含有する殺
虫、殺ダニ剤に存する。That is, the gist of the present invention resides in pyrazoles represented by the following general formula CI) and insecticides and acaricides containing the same as an active ingredient.
(上記式中、R1はメチル基又はエチル基を示し、Xは
ハロゲン原子、メチル基又はエチル基を示し、R2、R
3およびでは互いに独立してメチル基又はエチル基を示
す。)
以下、本発明の詳細な説明する。一般式(I)において
、R′はメチル基又はエチル基を示し、Xはフッ素原子
、塩素原子、臭素原子等のハロゲン原子;メチル基又は
エチル基を示し、好ましくはXは塩素原子又は臭素原子
である。R2、R3およびWは互いに独立してメチル基
又はエチル基を示し、好ましくはR2、R3および厭は
すべてメチル基である。具体例としては表−1記載の化
合物が挙げられるが、これらに限定されるものではない
。(In the above formula, R1 represents a methyl group or an ethyl group, X represents a halogen atom, a methyl group, or an ethyl group, R2, R
3 and independently represent a methyl group or an ethyl group. ) Hereinafter, the present invention will be explained in detail. In the general formula (I), R' represents a methyl group or an ethyl group, and X represents a halogen atom such as a fluorine atom, a chlorine atom, or a bromine atom; It is. R2, R3 and W each independently represent a methyl group or an ethyl group, preferably R2, R3 and all are methyl groups. Specific examples include, but are not limited to, the compounds listed in Table 1.
前記一般式(1)で表される本発明の化合物は例えば下
記反応式に従って製造することができる。The compound of the present invention represented by the general formula (1) can be produced, for example, according to the following reaction formula.
(II)
(I)
(上記反応式中、R1、R2、R3、R4およびXは前
記一般式CI)で定義したとおシであり、Zは塩素原子
、臭素原子、水酸基、メトキシ基、エトキシ基又はプロ
ポキシ基を示す。)
上記一般式(n)において、Zが塩素原子、臭素原子を
示す場合には、ベンゼン、トルエン又はキシレン等の芳
香族炭化水素;アセトン、メチルエチルケトン又はメチ
ルイソブチルケト/等のケトン類;クロロホルム又は塩
化メチレン等のハロゲン化炭化水素;水;酢酸メチル又
は酢酸エチル等のエステル類;テトラヒドロフラン、ア
セトニトリル、ジオキサン、 N、N−ジメチルホルム
アミド、N−メチルピロリドン又はジメチルスルホキシ
ド等の非プロトン性極性溶媒中、0−30℃好ましくは
o −t ’Cで塩基の存在下、一般式(III)を反
応させることによシ上記一般式CI)の化合物を得るこ
とができる。塩基としては、水酸化ナトリウム、水酸化
カリウム、炭酸ナトリウム、炭酸カリウム、ピリジン又
はトリエチルアミン等が挙げられる。(II) (I) (In the above reaction formula, R1, R2, R3, R4 and X are as defined in the above general formula CI), and Z is a chlorine atom, a bromine atom, a hydroxyl group, a methoxy group, an ethoxy group Or represents a propoxy group. ) In the above general formula (n), when Z represents a chlorine atom or a bromine atom, an aromatic hydrocarbon such as benzene, toluene or xylene; ketones such as acetone, methyl ethyl ketone or methyl isobutyl keto/etc.; chloroform or chloride; In halogenated hydrocarbons such as methylene; water; esters such as methyl acetate or ethyl acetate; aprotic polar solvents such as tetrahydrofuran, acetonitrile, dioxane, N,N-dimethylformamide, N-methylpyrrolidone or dimethylsulfoxide; The compound of the above general formula CI) can be obtained by reacting the general formula (III) in the presence of a base at -30°C, preferably o -t 'C. Examples of the base include sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, pyridine, and triethylamine.
また、一般式(n)において、Zが水酸基、メトキシ基
、エトキシ基又はプロポキシ基を示す場合には、無溶媒
又はN、N−ジメチルホルムアミド、N−メチルピロリ
ドン、ジメチルスルホキシド等の高沸点溶媒中、13θ
〜コSθ℃好ましくはコ00−2 S 0℃で、一般式
(III)の化合物を反応させることによシ上記一般式
(I)の化合物を得ることができる。In general formula (n), when Z represents a hydroxyl group, a methoxy group, an ethoxy group, or a propoxy group, it may be used without a solvent or in a high boiling point solvent such as N,N-dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide, etc. , 13θ
The compound of the above general formula (I) can be obtained by reacting the compound of the general formula (III) at ˜Sθ°C, preferably 0°C.
尚、上記一般式(n)で表される化合物は例えば、Bu
l 1. Soc、Chim、 France+土二ム
(19/、A)記載の方法に準じて製造することができ
る。In addition, the compound represented by the above general formula (n) is, for example, Bu
l 1. It can be produced according to the method described in Soc, Chim, France+Chim (19/, A).
一般式(I)で示される化合物は下記の鞘翅目、鱗翅目
、半翅目、直翅目、双翅目等の昆虫及び植物または動物
に寄生するダニ目の卵、幼虫に著しい防除活性を有する
が、勿論これらのみに限定されるものではない。The compound represented by the general formula (I) has remarkable control activity against the following insects of the orders Coleoptera, Lepidoptera, Hemiptera, Orthoptera, and Diptera, as well as the eggs and larvae of the order Acari that parasitize plants or animals. However, it is of course not limited to these.
7 半翅目;セジロウンカ、トビイロウンカ、ヒメトビ
ウンカ等のウンカ類、
ツマグロヨコバイ、オオヨコハイ
等のヨコバイ類、
モモアカアブラムシ等のアブラム
シ類
コ 鱗翅目;ハスモンヨトウ、ニカメイチユウ、コブノ
メイガ等
J 鞘翅目;アズキゾウムシ等
ダ 双翅目;イエバエ、ネツタイシマ力、アカイエカ等
5 ハダニ類;ナミハダニ、ニセナミハダニ、ミカンハ
ダニ等
6 マダニ類ニオウシマダニ、カズキダニ等の動物寄生
ダニ
一般式CI)で示される本発明の化合物を殺虫剤あるい
は殺ダニ剤として使用する場合には単独で用いてもよい
が、通常は従来の農薬と同様に補助剤を用いて乳剤、粉
剤、水利剤、液剤などの形態に製剤し、そのまま、ある
いは希釈して使用する。補助剤としては、殺虫剤の製剤
に用いられる通常のものが用いられる。例えばタルク、
カオリン、珪藻土、粘土、デンプンなどの固形担体、水
、シクロヘキサン、ベンゼン、キシレン、トルエン等の
炭化水素類、クロロベンゼンのようなハロゲン化炭化水
素類、エーテル類、ジメチルホルムアミド等のアミド類
、ケトン類、アルコール類、アセトニトリル等のニトリ
ル類などの溶媒、その他公知の乳化剤、分散剤などの界
面活性剤があげられる。7 Hemiptera: Planthoppers such as the brown planthopper, brown planthopper, and brown planthopper, leafhoppers such as the black leafhopper and giant leafhopper, and aphids such as the green peach aphid. Orders: House fly, Culex pipiens, Culex mosquito, etc. 5 Spider mites: Two-spotted spider mite, false red spider mite, Citrus spider mite, etc. 6 Ixodes: Animal parasitic mites such as Ixodes spp. When used, they may be used alone, but they are usually prepared in the form of emulsions, powders, irrigation agents, solutions, etc. using adjuvants like conventional agricultural chemicals, and used as they are or diluted. As adjuvants, those commonly used in insecticide formulations can be used. For example, talc,
Solid carriers such as kaolin, diatomaceous earth, clay, and starch, water, hydrocarbons such as cyclohexane, benzene, xylene, and toluene, halogenated hydrocarbons such as chlorobenzene, ethers, amides such as dimethylformamide, ketones, Examples include solvents such as alcohols and nitriles such as acetonitrile, and surfactants such as known emulsifiers and dispersants.
また、所望によっては他の殺虫剤、殺ダニ剤、殺菌剤、
昆虫生育調整物質、植物生育調整物質などと混用または
併用することも可能である。In addition, other insecticides, acaricides, fungicides,
It can also be mixed or used in combination with insect growth regulating substances, plant growth regulating substances, and the like.
製剤された殺虫殺ダニ剤中の有効成分濃度は、特に限定
されるものではないが、通常、粉剤ではO,S−20重
量%好ましくは7〜IO重量係、水利剤は/−?0重量
係好ましくは70〜g。The concentration of the active ingredient in the formulated insecticide and acaricide is not particularly limited, but is usually O,S-20% by weight for powders, preferably 7 to IO% by weight, and /-? for irrigation agents. 0 weight ratio, preferably 70-g.
重量%、乳剤は/−90重量%好ましくは10〜yoM
fitiyの有効成分を含有する。% by weight, the emulsion is /-90% by weight, preferably 10-yoM
Contains active ingredients of fitiy.
上記一般式(I)で示される化合物を殺虫剤として使用
する場合、通常活性成分が!;−1000ppm、好ま
しくは/ 0〜500 ppmの濃度範囲で使用する。When the compound represented by the above general formula (I) is used as an insecticide, the active ingredient is usually ! -1000 ppm, preferably in the concentration range of /0 to 500 ppm.
以下、本発明化合物の製造例、製剤例及び試験例によっ
て本発明を具体的に説明するが、本発明はその要旨を越
えない限り、以下の例に限定されるものではない。Hereinafter, the present invention will be specifically explained using production examples, formulation examples, and test examples of the compounds of the present invention, but the present invention is not limited to the following examples unless the gist thereof is exceeded.
製造例
N−(4’−)リメチルシリルペンジル〕−り一クロロ
ー3−エチル−7−メチル−ターヒラゾールカルボキサ
ミドの製造
グークロロ−3−エチル−/−メチル−ターピラゾール
カルボン酸/、g 9 ?と塩化チオニル6θ2を1時
間加熱還流した。塩化チオニルと減圧下留去後、残渣を
トルエン10m1に溶解した。これをクートリメチルシ
リルベンジルアミン/、7デ2のトルエン溶液20m1
中にO〜i。Production Example N-(4'-)limethylsilylpenzyl]-trichloro-3-ethyl-7-methyl-terhirazolecarboxamide Production of chloro-3-ethyl/-methyl-terpyrazolecarboxylic acid/, g 9? and thionyl chloride 6θ2 were heated under reflux for 1 hour. After thionyl chloride was distilled off under reduced pressure, the residue was dissolved in 10 ml of toluene. Add this to 20ml of a toluene solution of cootrimethylsilylbenzylamine/7de2.
O~i inside.
℃で滴下した。滴下後、2時間攪拌し氷水に注ぎ、トル
エンで抽出した。トルエン層を炭酸ナトリウム水溶液、
水、飽和食塩水にて洗浄した。It was added dropwise at ℃. After the dropwise addition, the mixture was stirred for 2 hours, poured into ice water, and extracted with toluene. Add toluene layer to sodium carbonate aqueous solution,
Washed with water and saturated saline.
無水硫酸ナトリウムで乾燥後、減圧上濃縮した。After drying over anhydrous sodium sulfate, it was concentrated under reduced pressure.
残渣をシリカゲルカラムクロマトグラフィーで精製し1
表−7記載の化合物()ffi / g ) J、 /
、5−9、n2; /、!r J A 7を得た。The residue was purified by silica gel column chromatography.
Compounds listed in Table-7 ()ffi/g) J,/
, 5-9, n2; /,! rJA7 was obtained.
得られた化合物のNMRおよびIRスペクトルを以下に
示す。The NMR and IR spectra of the obtained compound are shown below.
’HI’MFL(CC1,、)δppm ; o、コ5
(S、デH) /、2(t、、)H)uJl(q、2
H)K、0j(s、、?H)11.5(d、コH)
乙、9(b、/H)7.23Cd、2H)7.り5(d
、、2H)IR(CTL−リ; 3/7.ao、aqs
o、/乙60./jJ!;/!;J3. / +2’
l タ、 1ios、 gグO次に本発明化合物の
製剤例を示す。尚、以下に「部J、r%Jとあるのは、
それぞれ「重量部」、「重量部」を意味する。'HI'MFL(CC1,,)δppm; o, ko5
(S, deH) /,2(t,,)H)uJl(q,2
H) K, 0j (s,,?H) 11.5 (d, koH)
Otsu, 9(b, /H)7.23Cd,2H)7. ri5(d
,, 2H) IR (CTL-Re; 3/7.ao, aqs
o,/Otsu60. /jJ! ;/! ;J3. / +2'
Examples of formulations of the compounds of the present invention are shown below. In addition, below, "part J, r% J" means
They mean "parts by weight" and "parts by weight," respectively.
製剤例/ 製造例の化合物20部、カープレックス#g。Formulation example/ 20 parts of the compound of Preparation Example, Carplex #g.
(塩野義製薬社、商標名)20部、N、Nカオリンクレ
ー(上屋カオリン社、商標名)SS部、高級アルコール
硫酸エステル系界面活性剤ツルポールgo 7o (東
邦化学社、商標名)5部を配合し、均一に混合粉砕して
、有効成分に0%を含有する水利剤を得た。(Shionogi Pharmaceutical Co., Ltd., trade name) 20 parts, N, N kaolin clay (Ueya Kaolin Co., Ltd., trade name) SS part, higher alcohol sulfate ester surfactant Tsurupol go 7o (Toho Kagaku Co., Ltd., trade name) 5 parts were mixed and pulverized uniformly to obtain an aquarium containing 0% of active ingredients.
製剤例λ
製造例の本発明の化合物2部、クレー(日本り/’1社
g ) 93部、ホワイトカーボン5部を均一に混合粉
砕して、2俤粉剤を製造した。Formulation Example λ 2 parts of the compound of the present invention in Production Example, 93 parts of clay (Nihon Ri/'1 Co., Ltd.), and 5 parts of white carbon were uniformly mixed and pulverized to produce 2 powders.
製剤例3
製造例の本発明の化合物20部を、キシレン33部およ
びジメチルホルムアミド30部からなる混合溶媒に溶解
させ、これにポリオキシエチレン系界面活性剤ツルポー
ル3oosx(東邦化学社、商標名)75部を加えて、
有効成分、2θ係を含有する乳剤を得た。Formulation Example 3 20 parts of the compound of the present invention in Production Example was dissolved in a mixed solvent consisting of 33 parts of xylene and 30 parts of dimethylformamide, and the polyoxyethylene surfactant Tsurupol 3oosx (Toho Kagaku Co., Ltd., trade name) 75 was added to this. In addition,
An emulsion containing an active ingredient, 2θ modulus, was obtained.
製剤例グ
製造例の化合物30部、あらかじめ混合しておいたエチ
レングリコールg部、ツルポールAC,703,z(東
邦fヒ学社、商標名)5部、キサンタンガムo、i部を
水sb、q部に良く混合分散させた。次にこのスラリー
状混合物を、ダイノミル(シンマルエンターグライゼス
社〕で湿式粉砕して、有効成分30%を含有する安定な
フロアブル剤を得た。Formulation Example: 30 parts of the compound of the manufacturing example, g parts of ethylene glycol previously mixed, 5 parts of Tsurpol AC, 703, z (Toho Fhi Gakusha, trade name), o and i parts of xanthan gum, water sb and q. The mixture was well mixed and dispersed. Next, this slurry-like mixture was wet-milled using a Dyno Mill (Shinmaru Entergrise Co., Ltd.) to obtain a stable flowable agent containing 30% of the active ingredient.
試験例1 ナミハダニの成虫に対する効果インゲン葉の
リーフディスク(径2cm)に10頭のナミハダニ雌成
虫を成虫する。これに製剤例1の処決に従って製剤され
た本発明化合物を水で所定濃度に希釈しだ液Smlを、
回転式散布塔(みずは理化製)を用いて散布した。Test Example 1 Effect on adult two-spotted spider mites Ten female adult two-spotted spider mites are placed on a leaf disk (diameter 2 cm) of a kidney bean leaf. To this was added Sml of a saliva solution prepared by diluting the compound of the present invention prepared according to the procedure of Formulation Example 1 with water to a predetermined concentration.
Spraying was performed using a rotary spraying tower (manufactured by Mizuha Rika).
(/濃度、コ反復。)
処理2q時間後に、成虫の生死を調査し、殺ダニ率(%
)を求めた。その結果を表−一に示す。(Concentration, repetition.) After 2 q hours of treatment, the survival of the adults was investigated, and the acaricidal rate (%) was determined.
) was sought. The results are shown in Table 1.
試験例コ ナミハダニの卵に対する効果インゲン葉のリ
ーフディスク(径、2c!rL)に5頭のナミハダニ雌
成虫を成虫する。成虫後20時間リーフディスクに産卵
させ、その後雌成虫は除去した。これに、製剤例1の処
決に従って製剤された本発明化合物を水で所定濃度に希
釈しだ液5mlを回転式散布塔(みずは理化製)を用い
散布した。(l濃度、コ反復。)
処理5日後に未ふ化卵数とふ化幼虫数を調査し、殺卵率
(%)を求めた。その結果を表−一に示す。Test Example Effect on eggs of two-spotted spider mite Five adult female two-spotted spider mites are placed on a leaf disc (diameter, 2c!rL) of a kidney bean leaf. Eggs were allowed to lay on leaf discs for 20 hours after adulthood, and then the female adults were removed. To this, 5 ml of a saliva solution of the compound of the present invention prepared according to the procedure in Formulation Example 1 diluted with water to a predetermined concentration was sprayed using a rotary spray tower (manufactured by Mizuha Rika). (1 concentration, 3 repetitions.) Five days after the treatment, the number of unhatched eggs and the number of hatched larvae were investigated, and the ovicidal rate (%) was determined. The results are shown in Table 1.
試験例3 トビイロウンカの幼虫に対する効果ガラス円
筒(径3crn、長さ/7儂)に稲の芽出し苗をセクト
し、トビイロウンカグ令幼虫を5頭成虫する。これに、
製剤例3の処決に従って製剤された本発明の化合物を水
で希釈した液o、smlを、散布塔(みずは理化製〕を
用い散布した。(l濃度、を反復。)
処理29時間後に、幼虫の生死を調査し、殺虫率(俤)
を求めた。その結果を表−3に示す。Test Example 3 Effect on brown planthopper larvae Seed budding rice seedlings into a glass cylinder (diameter 3 crn, length/7 degrees), and collect 5 adult brown planthopper instar larvae. to this,
A solution o, sml of the compound of the present invention prepared according to the procedure in Formulation Example 3 diluted with water was sprayed using a scattering tower (manufactured by Mizuha Rika). (1 concentration was repeated.) 29 hours after treatment. , investigate whether the larvae are alive or dead, and determine the insect killing rate (忤)
I asked for The results are shown in Table-3.
試験例グ コナガの幼虫に対する効果
キャベツ切葉(!×Scr/L)を、製剤例1の処決に
従って製剤された本発明化合物を水で希釈した液に7分
間浸漬した。浸漬後風乾し、プラスチックカップ(径7
crn )に入れ、これにコナガの3令幼虫を5頭成
虫した。(l濃度、コ反復。ン
成虫2日後に幼虫の生死を調査し、殺虫率(チ)を求め
た。その結果を表−りに示す。Test Example G: Effect on diamondback moth larvae Cut cabbage leaves (!×Scr/L) were immersed in a solution prepared by diluting the compound of the present invention prepared according to the treatment in Formulation Example 1 with water for 7 minutes. After soaking, air dry and use a plastic cup (diameter 7
crn), and five adult diamondback moth 3rd instar larvae were placed therein. (Concentration: 1, repeat.) Two days after the adult larvae, the survival or death of the larvae was investigated, and the insecticidal rate (chi) was determined. The results are shown in the table.
表 −2
表−3
表
〔発明の効果〕
本発明のピラゾール類は優れた殺虫、殺ダニ効果を有し
ておシ、その価値は高い。Table 2 Table 3 Table [Effects of the Invention] The pyrazoles of the present invention have excellent insecticidal and acaricidal effects and are of high value.
Claims (3)
はハロゲン原子、メチル基又はエチル基を示し、R^2
、R^3及びR^4は互いに独立してメチル基又はエチ
ル基を示す。)(1) Pyrazole represented by the following general formula (I). ▲There are mathematical formulas, chemical formulas, tables, etc.▼・・・(I) (In the above formula, R^1 represents a methyl group or an ether group, and
represents a halogen atom, methyl group or ethyl group, R^2
, R^3 and R^4 each independently represent a methyl group or an ethyl group. )
3およびR^4がすべてメチル基であることを特徴とす
る請求項1に記載のピラゾール類。(2) X is a chlorine atom or a bromine atom, R^2, R^
The pyrazole according to claim 1, wherein 3 and R^4 are all methyl groups.
含有する殺虫、殺ダニ剤。(3) An insecticide or acaricide containing the pyrazole according to claim 1 as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63205251A JPH0253704A (en) | 1988-08-18 | 1988-08-18 | Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active component |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63205251A JPH0253704A (en) | 1988-08-18 | 1988-08-18 | Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active component |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0253704A true JPH0253704A (en) | 1990-02-22 |
Family
ID=16503893
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63205251A Pending JPH0253704A (en) | 1988-08-18 | 1988-08-18 | Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active component |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0253704A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024101630A1 (en) * | 2022-11-10 | 2024-05-16 | 삼성전자 주식회사 | Heat exchanger and air conditioner comprising same |
-
1988
- 1988-08-18 JP JP63205251A patent/JPH0253704A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024101630A1 (en) * | 2022-11-10 | 2024-05-16 | 삼성전자 주식회사 | Heat exchanger and air conditioner comprising same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR9905766B1 (en) | phthalamide derivative, pesticide, and process for using it. | |
JPH03128355A (en) | 4-acyloxyquinoline derivative and insecticide and acaricide containing the same derivative as active ingredient | |
JPH0262876A (en) | Pyrazoles and insecticide, acaricide and germicide containing pyrazoles as active ingredient | |
JPS60181067A (en) | Benzoylurea derivative, its preparation and insecticide | |
SU1501911A3 (en) | Versions of insecticide composition | |
CN109232550B (en) | 3-chloro-5-trifluoromethylpyridyl-1, 3, 4-oxadiazole-2-ketone compound and application thereof | |
JP3580594B2 (en) | Insecticidal fungicidal composition | |
JPH0253704A (en) | Trialkylsilylpyrazoles and insecticidal and miticidal agent containing same compound as active component | |
DK167012B1 (en) | FLUORO-SUBSTITUTED 3,4-DIPHENYL-1-PHENYL CARBAMOYL-2-PYRAZOLINES, PREPARING THEREOF AND USING IT AS AN INSECTICID AND ACARIZIDE EFFECT | |
JPH0421671A (en) | 4-pyrazolecarboxamides and insecticide and acaricide containing the same as active ingredient | |
JP2976038B2 (en) | Novel amidine derivative and insecticide and acaricide containing the same | |
JPH0368560A (en) | N-acyl-5-pyrazolecarboxamides and insecticide and acaricide containing the same as active ingredient | |
CN108299409B (en) | Phenylether oxadiazole pesticide | |
JPS63156765A (en) | Benzoylurea compound, insecticide and acaricide containing said compound as active ingredient | |
JPH02233679A (en) | Pyrazole compound and insecticide and acaricide containing the same as active ingredients | |
US4316044A (en) | Isovaleric acid derivatives | |
JPS6154765B2 (en) | ||
JPH0341004A (en) | Insecticidal and miticidal agent | |
JPS59106454A (en) | Novel urea derivative, its preparation and insecticidal composition | |
JPH02264760A (en) | 4-alkoxypyrazoles and insecticidal and miticidal agent containing the compound as active component | |
JPH02279662A (en) | Oxime ether and controller against harmful organism containing same ether | |
CN115894398A (en) | Fluorine-containing thiazole amide insecticide and acaricide | |
JPH0377861A (en) | Fluorine-containing sulfonamide derivative, insecticide and acaricide | |
JP3783353B2 (en) | Phosphorus compounds, their production methods and pesticides for agriculture and horticulture | |
JPS5920265A (en) | Benzoylurea derivative, its preparation and insecticidal and miticidal agent |