JPS62207250A - ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤 - Google Patents

ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤

Info

Publication number: JPS62207250A
Authority: JP; Japan
Prior art keywords: atom; tables; represented; compound according; following formula
Prior art date: 1986-02-28
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.): Granted

Application number

JP62045073A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0369338B2 (hu

Inventor

ヨーゼフ　ドラベック

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.)

Novartis AG

Original Assignee

Ciba Geigy AG

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.)

1986-02-28

Filing date

1987-02-27

Publication date

1987-09-11

1987-02-27 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1987-09-11 Publication of JPS62207250A publication Critical patent/JPS62207250A/ja

1991-10-31 Publication of JPH0369338B2 publication Critical patent/JPH0369338B2/ja

Status Granted legal-status Critical Current

Links

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238000005903 acid hydrolysis reaction Methods 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
230000001887 anti-feedant effect Effects 0.000 description 1
239000013011 aqueous formulation Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
229940097012 bacillus thuringiensis Drugs 0.000 description 1
239000002585 base Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
CIQSXZWTAAWJQY-UHFFFAOYSA-N benzyl-bis(2-chloroethyl)-ethylazanium Chemical compound ClCC[N+](CC)(CCCl)CC1=CC=CC=C1 CIQSXZWTAAWJQY-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
AOJDZKCUAATBGE-UHFFFAOYSA-N bromomethane Chemical compound Br[CH2] AOJDZKCUAATBGE-UHFFFAOYSA-N 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
159000000007 calcium salts Chemical class 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
150000001767 cationic compounds Chemical class 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000007931 coated granule Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229940125898 compound 5 Drugs 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
230000018109 developmental process Effects 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
HFPGRVHMFSJMOL-UHFFFAOYSA-N dibromomethane Chemical compound Br[CH]Br HFPGRVHMFSJMOL-UHFFFAOYSA-N 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940043264 dodecyl sulfate Drugs 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000010410 dusting Methods 0.000 description 1
244000078703 ectoparasite Species 0.000 description 1
239000003480 eluent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
125000005313 fatty acid group Chemical group 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
235000012055 fruits and vegetables Nutrition 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
230000012447 hatching Effects 0.000 description 1
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 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
230000002401 inhibitory effect Effects 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
230000013011 mating Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
239000012764 mineral filler Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
230000003151 ovacidal effect Effects 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
244000045947 parasite Species 0.000 description 1
230000002688 persistence Effects 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
125000005498 phthalate group Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229940113115 polyethylene glycol 200 Drugs 0.000 description 1
229940068918 polyethylene glycol 400 Drugs 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 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
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000002390 rotary evaporation Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000001119 stannous chloride Substances 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000003760 tallow Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1

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JP62045073A 1986-02-28 1987-02-27 ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤 Granted JPS62207250A (ja)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
CH808/86-7		1986-02-28
CH80886		1986-02-28
CH4617/86-9		1986-11-19
CH5238/86-6		1986-12-24

Related Child Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2341220A Division JPH0669994B2 (ja)	1986-02-28	1990-11-30	アニリン誘導体

Publications (2)

Publication Number	Publication Date
JPS62207250A true JPS62207250A (ja)	1987-09-11
JPH0369338B2 JPH0369338B2 (hu)	1991-10-31

Family

ID=4195666

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62045073A Granted JPS62207250A (ja)	1986-02-28	1987-02-27	ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤

Country Status (3)

Country	Link
JP (1)	JPS62207250A (hu)
MX (1)	MX5413A (hu)
ZA (1)	ZA871433B (hu)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH01168651A (ja) *	1987-12-01	1989-07-04	Bayer Ag	芳香核中及び側鎖中にフツ素原子を含むアルコキシアニリン及びその製造方法
JPH02155A (ja) *	1987-02-04	1990-01-05	Sumitomo Chem Co Ltd	ベンゾイル尿素誘導体、その製造法、その用途およびその中間体
JP2004149519A (ja) *	2002-10-07	2004-05-27	Ishihara Sangyo Kaisha Ltd	家屋害虫防除用組成物及び防除方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5289646A (en) *	1976-01-20	1977-07-27	Bayer Ag	New substituted nnphenylln* benzoyllurea and use thereof as insecticide
JPS53141242A (en) *	1977-05-13	1978-12-08	Dow Chemical Co	Substitution product of phenylaminocarbonyllbenzoamide
JPS55104258A (en) *	1979-02-01	1980-08-09	Ciba Geigy Ag	Substituted nn4433bromaryloxyphenyll nbenzoylureaits manufacture and noxious organism repellant containing it
JPS5826858A (ja) *	1981-07-30	1983-02-17	ザ・ダウ・ケミカル・カンパニ−	置換されたｎ‐アロイルｎ′‐フエニル尿素化合物およびその化合物を含む殺虫剤組成物
JPS61257958A (ja) *	1985-03-14	1986-11-15	イステイトウ−ト・グイド・ドネガニ・ソチエタ・ペル・アツイオニ	殺虫活性を有するベンゾイル尿素
JPS61277660A (ja) *	1985-06-04	1986-12-08	Nippon Soda Co Ltd	ベンゾイルウレア誘導体、その製造方法及び殺虫剤

1987
- 1987-02-27 ZA ZA871433A patent/ZA871433B/xx unknown
- 1987-02-27 JP JP62045073A patent/JPS62207250A/ja active Granted
- 1987-02-27 MX MX541387A patent/MX5413A/es unknown

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5289646A (en) *	1976-01-20	1977-07-27	Bayer Ag	New substituted nnphenylln* benzoyllurea and use thereof as insecticide
JPS53141242A (en) *	1977-05-13	1978-12-08	Dow Chemical Co	Substitution product of phenylaminocarbonyllbenzoamide
JPS55104258A (en) *	1979-02-01	1980-08-09	Ciba Geigy Ag	Substituted nn4433bromaryloxyphenyll nbenzoylureaits manufacture and noxious organism repellant containing it
JPS5826858A (ja) *	1981-07-30	1983-02-17	ザ・ダウ・ケミカル・カンパニ−	置換されたｎ‐アロイルｎ′‐フエニル尿素化合物およびその化合物を含む殺虫剤組成物
JPS61257958A (ja) *	1985-03-14	1986-11-15	イステイトウ−ト・グイド・ドネガニ・ソチエタ・ペル・アツイオニ	殺虫活性を有するベンゾイル尿素
JPS61277660A (ja) *	1985-06-04	1986-12-08	Nippon Soda Co Ltd	ベンゾイルウレア誘導体、その製造方法及び殺虫剤

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH02155A (ja) *	1987-02-04	1990-01-05	Sumitomo Chem Co Ltd	ベンゾイル尿素誘導体、その製造法、その用途およびその中間体
JPH01168651A (ja) *	1987-12-01	1989-07-04	Bayer Ag	芳香核中及び側鎖中にフツ素原子を含むアルコキシアニリン及びその製造方法
JP2004149519A (ja) *	2002-10-07	2004-05-27	Ishihara Sangyo Kaisha Ltd	家屋害虫防除用組成物及び防除方法

Also Published As

Publication number	Publication date
JPH0369338B2 (hu)	1991-10-31
ZA871433B (en)	1987-10-28
MX5413A (es)	1993-10-01

Legal Events

Date	Code	Title	Description
2003-10-31	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
JPH0347159A (ja)	1991-02-28	置換ｎ―ベンゾイル―ｎ′―２，５―ジクロロ―４―ヘキサフルオロプロピルオキシフェニル尿素の製造のための中間体
JPH0524144B2 (hu)	1993-04-06
JP2747824B2 (ja)	1998-05-06	置換されたｎ−ベンゾイル−ｎ’−２，５−ジハロー４−ペルフルオロアルコキシフェニル尿素、その製造方法及び有害生物防除におけるそれらの使用方法
KR910000252B1 (ko)	1991-01-23	해충방제에 유용한 벤조일페닐우레아의 제조방법
EP0231152A2 (de)	1987-08-05	Phenylbenzoylharnstoffe
KR900008136B1 (ko)	1990-10-31	벤조일페닐우레아의 제조 방법
JPS62207250A (ja)	1987-09-11	ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤
JPS6165859A (ja)	1986-04-04	Ｎ‐〔３‐ハロ‐４‐（ヘキサフルオロプロポキシ）‐５‐トリフルオロメチル〕フエニル‐ｎ′‐ベンゾイルウレア、その製造方法、それらを含有する有害生物防除剤、及びその使用方法
EP0138756A1 (de)	1985-04-24	Neue Oxadiazine
JP2719823B2 (ja)	1998-02-25	１―［４―（ハロフェノキシ）フェノキシ］―４―ペンチン、その製法およびその製造のための中間体
JPS63287761A (ja)	1988-11-24	Ｎ−ベンゾイル−ｎ′−トリハローハロアルコキシフェニル尿素，その製法および有害生物防除におけるその用途
JPH021452A (ja)	1990-01-05	ベンゾイルフェニル尿素、その製法および該化合物を含有する有害生物防除剤組成物
DE3320534A1 (de)	1983-12-15	Carbaminsaeureester
JPS6084250A (ja)	1985-05-13	しゆう酸アニリド、その製造方法及び有害生物を防除するためのその使用方法
JPS63179864A (ja)	1988-07-23	新規なジヒドロチアジアゾール及びこれを含有する有害生物防除剤
JPH0225458A (ja)	1990-01-26	ベンゾイルフェニル尿素
JPS6115879A (ja)	1986-01-23	新規なｎ‐フエニル‐ｎ‐テトラヒドロピラニル‐ｎ‐ベンゾイル尿素、その製法及び該化合物を含有する有害生物防除剤
JPS6197254A (ja)	1986-05-15	ベンゾイルフエニル尿素誘導体、その製造方法及び該化合物を有害生物の防除に用いる方法
JPS61151173A (ja)	1986-07-09	ベンゾイルフエニル尿素
JPS6197255A (ja)	1986-05-15	置換ｎ―ベンゾイル―ｎ’―２．５―ジクロロ―４―ヘキサフルオロプロピルオキシフェニル尿素、その製造方法及び該化合物を含有する組成物
JPS62106069A (ja)	1987-05-16	新規なベンゾイル尿素の塩、その製造方法及び有害生物防除方法
JPS6157545A (ja)	1986-03-24	置換ベンゾイルフエニル尿素、その製造方法及び該化合物を含有する有害生物防除剤
JPH01106855A (ja)	1989-04-24	Ｎ−ベンゾイル−ｎ’−２，４−ジフルオロ−３，５−ジハロフェニル尿素、それらの製法および有害生物防除におけるそれらの用途
JPS62185065A (ja)	1987-08-13	Ｎ−〔４−（ハロアルコキシ）トリフルオロメチルフエニル〕−ｎ′−ベンゾイル尿素、その製造方法及び有害生物を防除するためのその使用方法
HU197877B (en)	1989-06-28	Insecticide, acaricide and ovicide compositions containing phenyl-benzoyl-urea derivatives as active components and process for producing the active components

JPS62207250A - ベンゾイルフェニル尿素、その製造方法および該化合物を含有する殺虫、殺ダニ剤 - Google Patents

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Applications Claiming Priority (4)

Related Child Applications (1)

Publications (2)

Family

ID=4195666

Family Applications (1)

Country Status (3)

Cited By (3)

Citations (6)

Patent Citations (6)

Cited By (3)

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