PH26451A - Hydrazone compound and production therefor and an insecticidal composition containing the same - Google Patents

Hydrazone compound and production therefor and an insecticidal composition containing the same Download PDF

Info

Publication number: PH26451A
Authority: PH; Philippines
Prior art keywords: compound; hydrazone compound; acid; parts; hydrazone
Prior art date: 1988-08-26

Application number

PH39091A

Other languages

English (en)

Inventor

Hiroshi Kisida

Kenichi Mikitani

Yoko Torisu

Tomatoshi Imahase

Sumio Nishida

Original Assignee

Sumitomo Chemical Co

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.)

1988-08-26

Filing date

1989-08-14

Publication date

1992-07-15

1989-08-14 Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co

1992-07-15 Publication of PH26451A publication Critical patent/PH26451A/en

Links

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230000000749 insecticidal effect Effects 0.000 title claims description 16
-1 Hydrazone compound Chemical class 0.000 title description 63
238000004519 manufacturing process Methods 0.000 title description 17
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238000000034 method Methods 0.000 claims description 11
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239000003085 diluting agent Substances 0.000 claims description 4
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238000006243 chemical reaction Methods 0.000 description 16
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239000004563 wettable powder Substances 0.000 description 4
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150000001408 amides Chemical class 0.000 description 3
239000000440 bentonite Substances 0.000 description 3
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SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
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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 3
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235000010489 acacia gum Nutrition 0.000 description 1
239000001785 acacia senegal l. willd gum Substances 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000000783 alginic acid Substances 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
229960001126 alginic acid Drugs 0.000 description 1
150000004781 alginic acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
229910000148 ammonium phosphate Inorganic materials 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
239000001273 butane Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
239000001728 capsicum frutescens Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229960005286 carbaryl Drugs 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 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
235000021240 caseins Nutrition 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
235000013351 cheese Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000002385 cottonseed oil Substances 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
HCZKYJDFEPMADG-UHFFFAOYSA-N erythro-nordihydroguaiaretic acid Natural products C=1C=C(O)C(O)=CC=1CC(C)C(C)CC1=CC=C(O)C(O)=C1 HCZKYJDFEPMADG-UHFFFAOYSA-N 0.000 description 1
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000003112 inhibitor Substances 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
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
229960003951 masoprocol Drugs 0.000 description 1
ITNHSNMLIFFVQC-UHFFFAOYSA-N methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound COC(=O)C1C(C=C(C)C)C1(C)C ITNHSNMLIFFVQC-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
DHUNIARCLCYQGA-UHFFFAOYSA-N n'-amino-n,n-dimethylethanimidamide Chemical compound CN(C)C(C)=NN DHUNIARCLCYQGA-UHFFFAOYSA-N 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
150000004804 polysaccharides Chemical class 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920001592 potato starch Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
239000003380 propellant Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000010076 replication Effects 0.000 description 1
VEMKTZHHVJILDY-UHFFFAOYSA-N resmethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UHFFFAOYSA-N 0.000 description 1
VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
229940108410 resmethrin Drugs 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000008159 sesame oil Substances 0.000 description 1
235000011803 sesame oil Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
241000894007 species Species 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000012747 synergistic agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/76—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/69—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a carbon skeleton substituted by nitrogen atoms, not being part of nitro or nitroso groups
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
- C07C303/30—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reactions not involving the formation of esterified sulfo groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)

PH39091A 1988-08-26 1989-08-14 Hydrazone compound and production therefor and an insecticidal composition containing the same PH26451A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP21270388		1988-08-26

Publications (1)

Publication Number	Publication Date
PH26451A true PH26451A (en)	1992-07-15

Family

ID=16627032

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH39091A PH26451A (en)	1988-08-26	1989-08-14	Hydrazone compound and production therefor and an insecticidal composition containing the same

Country Status (13)

Country	Link
US (1)	US4980373A (tr)
EP (1)	EP0355832B1 (tr)
KR (1)	KR900003113A (tr)
AU (1)	AU616041B2 (tr)
BR (1)	BR8904288A (tr)
DE (1)	DE68903613T2 (tr)
EG (1)	EG18776A (tr)
ES (1)	ES2052850T3 (tr)
MY (1)	MY104162A (tr)
PH (1)	PH26451A (tr)
RU (1)	RU2002732C1 (tr)
TR (1)	TR24362A (tr)
ZA (1)	ZA896389B (tr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ241574A (en) *	1991-02-22	1993-08-26	Ishihara Sangyo Kaisha	Substituted phenyl derivatives of hydrazone and pesticidal compositions
IL105310A0 (en) *	1992-04-16	1993-08-18	Ciba Geigy Ag	Benzophenone derivatives
IL105208A0 (en) *	1992-04-23	1993-07-08	Sumitomo Chemical Co	Hydrazone derivatives,process for producing same,insecticides and/or acaricides containing same as active ingredient and intermediate compounds thereof
TW268881B (tr) *	1992-07-07	1996-01-21	Ciba Geigy Ag
JPH0841019A (ja) *	1994-05-27	1996-02-13	Nippon Bayeragrochem Kk	スルファミド誘導体、及び殺虫剤
IL117940A (en) *	1995-04-19	2003-06-24	Kumiai Chemical Industry Co	Benzylsulfide derivatives, process for their production and insecticide compositions containing them
EP0742202B1 (en) *	1995-05-12	1999-12-01	Nihon Bayer Agrochem K.K.	Benzophenone hydrazone derivatives as insecticides
DE19529612A1 (de) *	1995-08-11	1997-02-13	Merck Patent Gmbh	Sulfonyl- oder Sulfinyl-benzoylguanidin-Derivate
JP4204186B2 (ja) *	2000-11-24	2009-01-07	株式会社クラレ	立毛皮革様シートおよびその製造方法
US20080139574A1 (en)	2006-11-30	2008-06-12	Cadila Healthcare Limited	Novel quinoline derivatives
US8110608B2 (en)	2008-06-05	2012-02-07	Ecolab Usa Inc.	Solid form sodium lauryl sulfate (SLS) pesticide composition
US8968757B2 (en)	2010-10-12	2015-03-03	Ecolab Usa Inc.	Highly wettable, water dispersible, granules including two pesticides

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3375271A (en) *	1964-07-08	1968-03-26	Gen Aniline & Film Corp	Sun-screening compounds
US3732307A (en) *	1970-09-24	1973-05-08	Du Pont	Benzophenone hydrazones containing perfluoroalkyl,perfluoroalkoxy,and perfluoroalkylthio substituents
NZ189705A (en) *	1978-03-01	1981-07-13	Boots Co Ltd	Benzophenone-hydrazone derivatives and pesticidal compositions intermediates
GB2058057A (en) *	1979-08-31	1981-04-08	Boots Co Ltd	Pesticidal substituted benzophenone hydrazones

1989
- 1989-08-11 AU AU39556/89A patent/AU616041B2/en not_active Ceased
- 1989-08-12 MY MYPI89001102A patent/MY104162A/en unknown
- 1989-08-14 PH PH39091A patent/PH26451A/en unknown
- 1989-08-18 US US07/395,516 patent/US4980373A/en not_active Expired - Fee Related
- 1989-08-22 ZA ZA896389A patent/ZA896389B/xx unknown
- 1989-08-23 TR TR89/0778A patent/TR24362A/tr unknown
- 1989-08-24 EG EG41389A patent/EG18776A/xx active
- 1989-08-24 EP EP89115641A patent/EP0355832B1/en not_active Expired - Lifetime
- 1989-08-24 KR KR1019890012075A patent/KR900003113A/ko not_active Abandoned
- 1989-08-24 DE DE8989115641T patent/DE68903613T2/de not_active Expired - Fee Related
- 1989-08-24 ES ES89115641T patent/ES2052850T3/es not_active Expired - Lifetime
- 1989-08-25 BR BR898904288A patent/BR8904288A/pt not_active Application Discontinuation
- 1989-08-25 RU SU894742589A patent/RU2002732C1/ru active

Also Published As

Publication number	Publication date
TR24362A (tr)	1991-09-19
US4980373A (en)	1990-12-25
MY104162A (en)	1994-02-28
AU616041B2 (en)	1991-10-17
KR900003113A (ko)	1990-03-23
ZA896389B (en)	1990-05-30
DE68903613T2 (de)	1993-05-13
BR8904288A (pt)	1990-05-08
EG18776A (en)	1994-03-30
EP0355832A1 (en)	1990-02-28
EP0355832B1 (en)	1992-11-25
AU3955689A (en)	1990-03-01
ES2052850T3 (es)	1994-07-16
RU2002732C1 (ru)	1993-11-15
DE68903613D1 (de)	1993-01-07

Publication	Publication Date	Title
CA2239081C (en)	2006-01-31	Novel 5-amino-3-cyano-4-ethylsulfinyl-1-phenyl-pyrazole compounds and their use as pesticides
US5225443A (en)	1993-07-06	Insecticidal N'-substituted-N'-substituted N,N'-diacylhydrazines
KR840000764B1 (ko)	1984-06-08	벤조페논 히드라존의 제조방법
US4980373A (en)	1990-12-25	Hydrazone compound and production therefor, and an insecticidal composition containing the same
DE3779814T2 (de)	1993-02-04	Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine.
KR910000856B1 (ko)	1991-02-11	살충제 n'-치환-n-알킬카르보닐-n-아실히드라진
DE68908789T2 (de)	1994-04-14	Insectizide N'-substituierte-N-alkylcarbonyl-N'-acylhydrazine und N'-substituierte-N-acyl-N'-alkylcarbonyl hydrazine.
CZ410489A3 (cs)	1999-04-14	N-Fenylpyrazol-4-ylderiváty, insekticidní prostředky tyto látky obsahující a jejich použití k hubení hmyzu
JPH0798806B2 (ja)	1995-10-25	Ｎ′−置換−ｎ，ｎ′−置換ジアシルヒドラジンの６員複素環式誘導体
KR950005199B1 (ko)	1995-05-19	N'-치환된-n,n'-디아실히드라진의 6원 헤테로 고리 유도체
FI97616B (fi)	1996-10-15	2-fenyyli-imidatsolijohdannainen, sen valmistusmenetelmä ja käyttö niveljalkaistuholaisten torjuntaan
US4439440A (en)	1984-03-27	1-Alkoxycarbonylphenylcarbamoyl-3-phenyl-4-cyanoalkyl-2-pyrazolines and use as insecticides
EP0360098B1 (en)	1994-03-30	Benzimidazole derivatives, and their production and use
IE59962B1 (en)	1994-05-04	Five-membered heterocyclic derivatives of n'-substituted-n, n'-diacylhydrazines
KR0128285B1 (ko)	1998-04-02	피라졸 화합물, 그의 제조 및 용도
JPS6365069B2 (tr)	1988-12-14
JPS6326757B2 (tr)	1988-05-31
US7592374B2 (en)	2009-09-22	Insecticidal nitromethylene compounds
US4539328A (en)	1985-09-03	Nematicidal isothiazole derivatives
JPS6314713B2 (tr)	1988-04-01
JP2715587B2 (ja)	1998-02-18	ヒドラゾン系化合物およびそれを有効成分とする殺虫剤
US3962444A (en)	1976-06-08	Use of 4-thiocyano-quinazolines as fungicides
JP2715583B2 (ja)	1998-02-18	ヒドラゾン系化合物およびそれを有効成分とする殺虫剤
KR870001946B1 (ko)	1987-10-23	트리할로 이미다졸 유도체의 제조방법
JPH01146870A (ja)	1989-06-08	ベンゾイル尿素誘導体、その用途およびその中間体