JPH0442376B2 - - Google Patents

Info

Publication number: JPH0442376B2
Authority: JP; Japan
Prior art keywords: alkyl group; lower alkyl; compound; general formula; formula
Prior art date: 1984-07-06
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.): Expired - Lifetime

Application number

JP59138955A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6118751A (ja

Inventor

Yoshio Kurahashi

Kozo Shiokawa

Shinzo Toshibe

Shinji Sakawa

Koichi Moriie

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

NIPPON BAIERU AGUROKEMU KK

Original Assignee

NIPPON BAIERU AGUROKEMU KK

Priority date (The priority date 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 date listed.)

1984-07-06

Filing date

1984-07-06

Publication date

1992-07-13

1984-07-06 Application filed by NIPPON BAIERU AGUROKEMU KK filed Critical NIPPON BAIERU AGUROKEMU KK

1984-07-06 Priority to JP59138955A priority Critical patent/JPS6118751A/ja

1985-06-20 Priority to EP85107613A priority patent/EP0170842B1/de

1985-06-20 Priority to DE8585107613T priority patent/DE3572971D1/de

1985-07-01 Priority to KR1019850004704A priority patent/KR920002790B1/ko

1985-07-01 Priority to BR8503154A priority patent/BR8503154A/pt

1986-01-27 Publication of JPS6118751A publication Critical patent/JPS6118751A/ja

1986-04-09 Priority to US06/850,462 priority patent/US4710518A/en

1990-06-25 Priority to US07/543,259 priority patent/US5061731A/en

1991-09-05 Priority to US07/755,257 priority patent/US5117053A/en

1992-07-13 Publication of JPH0442376B2 publication Critical patent/JPH0442376B2/ja

Status Granted legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 claims description 67
125000000217 alkyl group Chemical group 0.000 claims description 32
125000005843 halogen group Chemical group 0.000 claims description 22
238000004519 manufacturing process Methods 0.000 claims description 20
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
230000000855 fungicidal effect Effects 0.000 claims description 9
WPETWIRCSJXPAN-UHFFFAOYSA-N n-benzylcyclopropanecarboxamide Chemical class C1CC1C(=O)NCC1=CC=CC=C1 WPETWIRCSJXPAN-UHFFFAOYSA-N 0.000 claims description 8
239000004480 active ingredient Substances 0.000 claims description 7
239000000417 fungicide Substances 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
ADENQGQWSPPCDL-UHFFFAOYSA-N 1-benzylcyclopropane-1-carboxamide Chemical class C=1C=CC=CC=1CC1(C(=O)N)CC1 ADENQGQWSPPCDL-UHFFFAOYSA-N 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 27
201000010099 disease Diseases 0.000 description 24
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 24
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
-1 ligroin Chemical compound 0.000 description 19
238000000034 method Methods 0.000 description 15
239000000203 mixture Substances 0.000 description 14
239000000843 powder Substances 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
241000209094 Oryza Species 0.000 description 11
235000007164 Oryza sativa Nutrition 0.000 description 11
239000003795 chemical substances by application Substances 0.000 description 11
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 11
235000009566 rice Nutrition 0.000 description 11
230000015572 biosynthetic process Effects 0.000 description 10
238000003786 synthesis reaction Methods 0.000 description 10
238000012360 testing method Methods 0.000 description 9
241000196324 Embryophyta Species 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
229920003171 Poly (ethylene oxide) Polymers 0.000 description 7
244000052769 pathogen Species 0.000 description 7
238000002360 preparation method Methods 0.000 description 7
239000002904 solvent Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000003905 agrochemical Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
239000004927 clay Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000008187 granular material Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000003085 diluting agent Substances 0.000 description 5
235000019441 ethanol Nutrition 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000007921 spray Substances 0.000 description 5
238000005507 spraying Methods 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
241000233866 Fungi Species 0.000 description 4
239000004372 Polyvinyl alcohol Substances 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
229920002451 polyvinyl alcohol Polymers 0.000 description 4
235000019422 polyvinyl alcohol Nutrition 0.000 description 4
239000002994 raw material Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 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
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
239000005909 Kieselgur Substances 0.000 description 3
241001330975 Magnaporthe oryzae Species 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
239000000443 aerosol Substances 0.000 description 3
230000000844 anti-bacterial effect Effects 0.000 description 3
230000004071 biological effect Effects 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000013078 crystal Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000945 filler Substances 0.000 description 3
125000001153 fluoro group Chemical group F* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
238000010998 test method Methods 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
VVQBCJVUHJFBRM-UHFFFAOYSA-N 1,2,2-trichloro-3,3-dimethylcyclopropane-1-carbonyl chloride Chemical compound CC1(C)C(Cl)(Cl)C1(Cl)C(Cl)=O VVQBCJVUHJFBRM-UHFFFAOYSA-N 0.000 description 2
YHFWBUTYFKNBJR-UHFFFAOYSA-N 1,2,2-trichloro-3,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(Cl)(Cl)C1(Cl)C(O)=O YHFWBUTYFKNBJR-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
241000235349 Ascomycota Species 0.000 description 2
241000221198 Basidiomycota Species 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000003973 alkyl amines Chemical class 0.000 description 2
125000005037 alkyl phenyl group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
229940072049 amyl acetate Drugs 0.000 description 2
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
244000052616 bacterial pathogen Species 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
125000001246 bromo group Chemical group Br* 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
239000002734 clay mineral Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 2
238000007865 diluting Methods 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 2
239000005457 ice water Substances 0.000 description 2
239000003701 inert diluent Substances 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
238000011081 inoculation Methods 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 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
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
NTMJDABWJARASG-ARJAWSKDSA-N methyl (z)-2-chlorobut-2-enoate Chemical compound COC(=O)C(\Cl)=C\C NTMJDABWJARASG-ARJAWSKDSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000003380 propellant Substances 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
230000000391 smoking effect Effects 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
150000003462 sulfoxides Chemical class 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 2
WWYNJERNGUHSAO-XUDSTZEESA-N (+)-Norgestrel Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 WWYNJERNGUHSAO-XUDSTZEESA-N 0.000 description 1
AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
MVIJYGPBJJYXCR-UHFFFAOYSA-N 1,2,2-trichloro-3,3-diethylcyclopropane-1-carboxylic acid Chemical compound CCC1(CC)C(Cl)(Cl)C1(Cl)C(O)=O MVIJYGPBJJYXCR-UHFFFAOYSA-N 0.000 description 1
AORGWNNCEGYUCZ-UHFFFAOYSA-N 1,2,2-trichloro-n-[1-(4-chlorophenyl)ethyl]-3,3-dimethylcyclopropane-1-carboxamide Chemical compound C=1C=C(Cl)C=CC=1C(C)NC(=O)C1(Cl)C(C)(C)C1(Cl)Cl AORGWNNCEGYUCZ-UHFFFAOYSA-N 0.000 description 1
PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
RJPLGQTZHLRZGX-UHFFFAOYSA-N 1-(2-chlorophenyl)ethanamine Chemical compound CC(N)C1=CC=CC=C1Cl RJPLGQTZHLRZGX-UHFFFAOYSA-N 0.000 description 1
UJUFOUVXOUYYRG-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)ethanamine Chemical compound CC(N)C1=CC=C(Cl)C(Cl)=C1 UJUFOUVXOUYYRG-UHFFFAOYSA-N 0.000 description 1
SOZMSEPDYJGBEK-UHFFFAOYSA-N 1-(4-bromophenyl)ethanamine Chemical compound CC(N)C1=CC=C(Br)C=C1 SOZMSEPDYJGBEK-UHFFFAOYSA-N 0.000 description 1
PINPOEWMCLFRRB-UHFFFAOYSA-N 1-(4-chlorophenyl)ethanamine Chemical compound CC(N)C1=CC=C(Cl)C=C1 PINPOEWMCLFRRB-UHFFFAOYSA-N 0.000 description 1
IVKPXWBUKVTLHH-UHFFFAOYSA-N 1-bromo-2,2-dichloro-3,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(Cl)(Cl)C1(Br)C(O)=O IVKPXWBUKVTLHH-UHFFFAOYSA-N 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 1
QXAXQSMPKUHBQT-UHFFFAOYSA-N 2,2-dichloro-1-fluoro-3,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(F)(C(O)=O)C1(Cl)Cl QXAXQSMPKUHBQT-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
229910021532 Calcite Inorganic materials 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
241000222235 Colletotrichum orbiculare Species 0.000 description 1
240000008067 Cucumis sativus Species 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
239000004368 Modified starch Substances 0.000 description 1
229920000881 Modified starch Polymers 0.000 description 1
CCKSLAUZQQZXKD-UHFFFAOYSA-M O.[Na+].[O-]Br=O Chemical compound O.[Na+].[O-]Br=O CCKSLAUZQQZXKD-UHFFFAOYSA-M 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
229920001213 Polysorbate 20 Polymers 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
229910021536 Zeolite Inorganic materials 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
150000003869 acetamides Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001346 alkyl aryl ethers Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
229910021417 amorphous silicon Inorganic materials 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000003443 antiviral agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000005667 attractant Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
125000005997 bromomethyl group Chemical group 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
235000011116 calcium hydroxide Nutrition 0.000 description 1
VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
239000002775 capsule Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
229940071162 caseinate Drugs 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
AIMMVWOEOZMVMS-UHFFFAOYSA-N cyclopropanecarboxamide Chemical class NC(=O)C1CC1 AIMMVWOEOZMVMS-UHFFFAOYSA-N 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
229940099364 dichlorofluoromethane Drugs 0.000 description 1
QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
238000010410 dusting Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
238000003958 fumigation Methods 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000001727 glucose Nutrition 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
229960004592 isopropanol Drugs 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
238000004898 kneading Methods 0.000 description 1
230000003902 lesion Effects 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000011419 magnesium lime Substances 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
OVNLPNMCVJZSTA-ARJAWSKDSA-N methyl (z)-2-fluorobut-2-enoate Chemical compound COC(=O)C(\F)=C\C OVNLPNMCVJZSTA-ARJAWSKDSA-N 0.000 description 1
SOYGMDUAMIUEMQ-UHFFFAOYSA-N methyl 1,2,2-trichloro-3,3-dimethylcyclopropane-1-carboxylate Chemical compound COC(=O)C1(Cl)C(C)(C)C1(Cl)Cl SOYGMDUAMIUEMQ-UHFFFAOYSA-N 0.000 description 1
MEDDKYUDANFLRP-UHFFFAOYSA-N methyl 2-chloro-3-ethylpent-2-enoate Chemical compound CCC(CC)=C(Cl)C(=O)OC MEDDKYUDANFLRP-UHFFFAOYSA-N 0.000 description 1
XRLANTGFLPFPRV-UHFFFAOYSA-N methyl 2-chloro-3-methylbut-2-enoate Chemical compound COC(=O)C(Cl)=C(C)C XRLANTGFLPFPRV-UHFFFAOYSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
235000019426 modified starch Nutrition 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
150000004045 organic chlorine compounds Chemical class 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003444 phase transfer catalyst Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000008262 pumice Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
NYCVSSWORUBFET-UHFFFAOYSA-M sodium;bromite Chemical compound [Na+].[O-]Br=O NYCVSSWORUBFET-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
229940029284 trichlorofluoromethane Drugs 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1
239000010457 zeolite Substances 0.000 description 1

JP59138955A 1984-07-02 1984-07-06 Ｎ―ベンジル―シクロプロパンカルボキサミド誘導体、その製法及び農園芸用殺菌剤 Granted JPS6118751A (ja)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
JP59138955A JPS6118751A (ja)	1984-07-06	1984-07-06	Ｎ―ベンジル―シクロプロパンカルボキサミド誘導体、その製法及び農園芸用殺菌剤
EP85107613A EP0170842B1 (de)	1984-07-02	1985-06-20	N-Benzylcyclopropancarboxamid-Derivate, Verfahren zu ihrer Herstellung und Fungizide für Landwirtschaft und Gartenbau
DE8585107613T DE3572971D1 (en)	1984-07-02	1985-06-20	N-benzylcyclopropanecarboxamide derivatives, process for their preparation and fungicides for agriculture and horticulture
KR1019850004704A KR920002790B1 (ko)	1984-07-02	1985-07-01	N-벤질-사이클로프로판 카복스아미드 유도체의 제조방법
BR8503154A BR8503154A (pt)	1984-07-02	1985-07-01	Derivados de n-benzilciclopropanocar boxamida,processo para a sua preparacao,aplicacao,composicoes e processo para combater fungos,processo para a preparacao de composicoes e derivados de acido ciclopropanocarboxilico
US06/850,462 US4710518A (en)	1984-07-02	1986-04-09	Novel N-benzyl-cyclopropanecarboxamide fungicides
US07/543,259 US5061731A (en)	1984-07-02	1990-06-25	Novel n-benzyl-cyclopropanecarboxamide fungicides
US07/755,257 US5117053A (en)	1984-07-02	1991-09-05	N-benzyl-cyclopropanecarboxamide fungicides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59138955A JPS6118751A (ja)	1984-07-06	1984-07-06	Ｎ―ベンジル―シクロプロパンカルボキサミド誘導体、その製法及び農園芸用殺菌剤

Related Child Applications (1)

Application Number	Title	Priority Date	Filing Date
JP18286491A Division JPH059151A (ja)	1991-06-29	1991-06-29	シクロプロパンカルボン酸誘導体

Publications (2)

Publication Number	Publication Date
JPS6118751A JPS6118751A (ja)	1986-01-27
JPH0442376B2 true JPH0442376B2 (zh)	1992-07-13

Family

ID=15234066

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59138955A Granted JPS6118751A (ja)	1984-07-02	1984-07-06	Ｎ―ベンジル―シクロプロパンカルボキサミド誘導体、その製法及び農園芸用殺菌剤

Country Status (1)

Country	Link
JP (1)	JPS6118751A (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0784426B2 (ja) *	1986-08-25	1995-09-13	日本バイエルアグロケム株式会社	シクロプロパンカルボキサミド及び農業用殺菌剤
JP2553335B2 (ja) *	1986-08-25	1996-11-13	日本バイエルアグロケム株式会社	光学活性シクロプロパンカルボキサミド類及び該活性体とその鏡像異性体との鏡像異性体対、並びに農業用殺菌剤

1984
- 1984-07-06 JP JP59138955A patent/JPS6118751A/ja active Granted

Also Published As

Publication number	Publication date
JPS6118751A (ja)	1986-01-27

Publication	Publication Date	Title
JPH0378383B2 (zh)	1991-12-13
JPS6139941B2 (zh)	1986-09-06
KR920002790B1 (ko)	1992-04-03	N-벤질-사이클로프로판 카복스아미드 유도체의 제조방법
US5117053A (en)	1992-05-26	N-benzyl-cyclopropanecarboxamide fungicides
JPH0149344B2 (zh)	1989-10-24
JPH0442376B2 (zh)	1992-07-13
JPS6097964A (ja)	1985-05-31	Ν−キノキザリルアニリン系化合物，その製造法および農園芸用殺菌，殺虫，殺ダニ剤
JPH0231066B2 (zh)	1990-07-11
JPS62201855A (ja)	1987-09-05	カルボキサミド類、その製法及び農業用殺菌剤
JP4712261B2 (ja)	2011-06-29	ヒドラゾン誘導体および有害生物防除剤
JPS6160659A (ja)	1986-03-28	置換フエニルスルホニルアゾ−ル、その製法及び農園芸用殺菌剤
JP2553335B2 (ja)	1996-11-13	光学活性シクロプロパンカルボキサミド類及び該活性体とその鏡像異性体との鏡像異性体対、並びに農業用殺菌剤
KR920002793B1 (ko)	1992-04-03	벤질우레아 유도체의 제조방법
JPS6036478A (ja)	1985-02-25	クマリン酸エステル、その製法及び農園芸用殺菌剤
JPS6021135B2 (ja)	1985-05-25	トルイル酸アニリド類及びその製造方法並びにそれを含有する農園芸用殺菌剤
JPS6078966A (ja)	1985-05-04	トリクロルアクリロイルオキシム誘導体，その製法及び農業用殺菌剤
JPH0519551B2 (zh)	1993-03-17
JPS59101403A (ja)	1984-06-12	カルボン酸２，２−ジクロル−３，３−ジメチル−シクロプロピルメチルエステル誘導体及び農業用殺菌剤
JPS6350350B2 (zh)	1988-10-07
JPS5821672A (ja)	1983-02-08	ベンゾイソチアゾ−ル誘導体、その製法、及び農業用殺菌剤
JPS6323988B2 (zh)	1988-05-18
JPS5815965A (ja)	1983-01-29	ベンゾイソチアゾ−ル誘導体並びにその塩酸塩、その製法、及び農業用殺菌剤
JPH0784426B2 (ja)	1995-09-13	シクロプロパンカルボキサミド及び農業用殺菌剤
KR820000055B1 (ko)	1982-02-06	우레아 또는 티오우레아 화합물의 제조방법
JPS59101453A (ja)	1984-06-12	２，２−ジクロル−３，３−ジメチルシクロプロピルメチルカ−バメ−ト誘導体、並びに農業用殺菌剤