KR900016149A - 살충·살비 활성의 피리다지논 - Google Patents
살충·살비 활성의 피리다지논 Download PDFInfo
- Publication number
- KR900016149A KR900016149A KR1019900004666A KR900004666A KR900016149A KR 900016149 A KR900016149 A KR 900016149A KR 1019900004666 A KR1019900004666 A KR 1019900004666A KR 900004666 A KR900004666 A KR 900004666A KR 900016149 A KR900016149 A KR 900016149A
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- KR
- South Korea
- Prior art keywords
- chloro
- pyridazinone
- butyl
- group
- benzylthio
- Prior art date
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- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 title claims 7
- 230000000895 acaricidal effect Effects 0.000 title 1
- 239000000642 acaricide Substances 0.000 title 1
- 230000000694 effects Effects 0.000 title 1
- 230000000749 insecticidal effect Effects 0.000 title 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 229910052724 xenon Inorganic materials 0.000 claims 3
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims 3
- -1 1,1,2-trifluoro-2-trifluoromethoxyethoxy Chemical group 0.000 claims 2
- 241000607479 Yersinia pestis Species 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- GMBLXPQEVGTPEW-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[1-[4-(2,2-dichloroethenyl)phenyl]ethylsulfanyl]pyridazin-3-one Chemical compound C=1C=C(C=C(Cl)Cl)C=CC=1C(C)SC=1C=NN(C(C)(C)C)C(=O)C=1Cl GMBLXPQEVGTPEW-UHFFFAOYSA-N 0.000 claims 1
- YBOZCLOBAGGJNJ-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[1-[4-(2-chloro-3,3,3-trifluoroprop-1-enyl)phenyl]ethylsulfanyl]pyridazin-3-one Chemical compound C=1C=C(C=C(Cl)C(F)(F)F)C=CC=1C(C)SC=1C=NN(C(C)(C)C)C(=O)C=1Cl YBOZCLOBAGGJNJ-UHFFFAOYSA-N 0.000 claims 1
- LSABEBRBCHSUSU-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[1-[4-[1,2-difluoro-2-(trifluoromethoxy)ethenyl]phenyl]ethylsulfanyl]pyridazin-3-one Chemical compound C=1C=C(C(F)=C(F)OC(F)(F)F)C=CC=1C(C)SC=1C=NN(C(C)(C)C)C(=O)C=1Cl LSABEBRBCHSUSU-UHFFFAOYSA-N 0.000 claims 1
- ZMYHEAZHQIMJGY-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[[4-(2-chloro-2-phenylethenyl)phenyl]methylsulfanyl]pyridazin-3-one Chemical compound O=C1N(C(C)(C)C)N=CC(SCC=2C=CC(C=C(Cl)C=3C=CC=CC=3)=CC=2)=C1Cl ZMYHEAZHQIMJGY-UHFFFAOYSA-N 0.000 claims 1
- LAOCNTUEEBGRGM-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[[4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]phenyl]methoxy]pyridazin-3-one Chemical compound O=C1N(C(C)(C)C)N=CC(OCC=2C=CC(OC(F)(F)C(F)OC(F)(F)F)=CC=2)=C1Cl LAOCNTUEEBGRGM-UHFFFAOYSA-N 0.000 claims 1
- RDLNUKRLHCZDMS-UHFFFAOYSA-N 2-tert-butyl-4-chloro-5-[[4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]phenyl]methylsulfanyl]pyridazin-3-one Chemical compound O=C1N(C(C)(C)C)N=CC(SCC=2C=CC(OC(F)(F)C(F)OC(F)(F)F)=CC=2)=C1Cl RDLNUKRLHCZDMS-UHFFFAOYSA-N 0.000 claims 1
- TXESQUPGIGUQGU-UHFFFAOYSA-N 4-chloro-2-(3,4-dichlorophenyl)-5-[[4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]phenyl]methoxy]pyridazin-3-one Chemical compound C1=CC(OC(F)(F)C(OC(F)(F)F)F)=CC=C1COC1=C(Cl)C(=O)N(C=2C=C(Cl)C(Cl)=CC=2)N=C1 TXESQUPGIGUQGU-UHFFFAOYSA-N 0.000 claims 1
- AFBSCFAPIJGHKL-UHFFFAOYSA-N 4-chloro-2-(3,4-dichlorophenyl)-5-[[4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]phenyl]methylsulfanyl]pyridazin-3-one Chemical compound C1=CC(OC(F)(F)C(OC(F)(F)F)F)=CC=C1CSC1=C(Cl)C(=O)N(C=2C=C(Cl)C(Cl)=CC=2)N=C1 AFBSCFAPIJGHKL-UHFFFAOYSA-N 0.000 claims 1
- 241000238876 Acari Species 0.000 claims 1
- CBLGYOHCPHRYIP-UHFFFAOYSA-N CC(C)(C)N1C(=O)C(=C(C=N1)SCC2=CC=C(C=C2)C=C(C3=CC=C(C=C3)Cl)Cl)Cl Chemical compound CC(C)(C)N1C(=O)C(=C(C=N1)SCC2=CC=C(C=C2)C=C(C3=CC=C(C=C3)Cl)Cl)Cl CBLGYOHCPHRYIP-UHFFFAOYSA-N 0.000 claims 1
- 241001465754 Metazoa Species 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 1
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 150000007529 inorganic bases Chemical class 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 244000144972 livestock Species 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 150000007530 organic bases Chemical class 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 230000035515 penetration Effects 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
Classifications
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/14—Oxygen atoms
- C07D237/16—Two oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/18—Sulfur atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (24)
- 일반식(I)의 피리다지논[상기식에서, R은 직쇄 또는 측쇄(C2~C6)알킬기 : 할로겐원자, 저급알킬, 할로알킬, 알콕시, 할로알콕시기로 치환될 수 있는 페닐기를 나타내고; X는 할로겐원자를 나타내며, Y는 산소원자나 황원자 또는 NH기를 나타내고; B는를 나타내며; b는 0 또는 1이고; R1, R2, R3및 R4은 각각 독립적으로 H, 직쇄 또는 측쇄(C1~C4)알킬 또는 할로알킬기를 나타내며; Z는 CH기 또는 N원자를 나타내고; Y1는 O, S, CO 또는(식중, Rk및 Rj는 각각 독립적으로 H, 직쇄 또는 측쇄(C1~C4)알킬 또는 할로알킬기이다)를 나타내며; W는 직쇄 또는 측쇄(C2~C6) 할로알킬렌을 나타내고; y 및 w는 각각 독립적으로 0또는 1이며; Rx는 W=0일 때 치환체로서C1~C3할로알콕시 또는 페닐기(페닐기는 할로겐원자, (C1~C6)알킬, 할로알킬, 알콕시, 할로알콕시기로 이루어진 회전 치환체를 함유할 수 있다)를 함유할 수 있는 직쇄 또는 측쇄(C2~C6)할로알케닐기; (C1~C4)알킬 또는 할로알킬기로 이루어진 치환체를 함유할 수 있는 (C3~C6) 할로시클로알킬기 또는 (C4~C7)할로시클로알킬알킬기를 나타내며; w=1일때는 직쇄 또는 측쇄(C1~C6)할로알킬기를 나타내고; R′은 할로겐원자를 나타내며; n은 0, 1, 2이고; n이 2일때는 R′기는 동일하건 서로 다를 수 있다.]
- 제1항에 있어서, 하기 일반식(Ia)의 피리다지논.[상기식에서, R은 (C2~C6) 알킬기를 나타내고; X는 할로겐을 나타내며; Y는 O, S를 나타내고; 그 밖의 다른 부호는 제1항에서 정의한 바와 같다.]
- 2-t-부틸-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-α-메틸벤질옥시]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-α-메틸벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-벤질옥시]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-펜타플루오로에톡시-1,1,2-트리플루오로메톡시)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-펜타플루오로에톡시-1,1,2-트리플루오로메톡시)-α-메틸벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-클로로-3,3,3-트리플루오로프로메톡시)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2,2-디클로로에테닐(0벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,1,2-트리플루오로)-2-트리플루오로메톡시에톡시)-에틸)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,2-디플루오로)-2-트리플루오로메톡시에톡시)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-클로로-3,3,3-트리플루오로프로페닐)-α-메틸벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2,2-디클로로에테닐)-α-메틸벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(1,2-디플루오로-2-트리플루오로메톡시에테닐)-α-메틸벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-클로로-2-페닐에테닐)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2-클로로-(4-클로로페닐)-에테닐)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2,2-디클로로-1-메틸시클로로프로필메톡시)-벤질티오]-3(2H)-피리다지논.
- 2-t-부틸-4-클로로-5-[4-(2,2-디클로로-1-메틸시클로로프로필카르보닐)-벤질티오]-3(2H)-피리다지논.
- 2-(3,4-디클로로페닐)-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-벤질옥시]-3(2H)-피리다지논.
- 2-(3,4-디클로로페닐)-4-클로로-5-[4-(1,1,2-트리플루오로-2-트리플루오로메톡시에톡시)-벤질티오]-3(2H)-피리다지논.
- 유기비힐클중, 무기 또는 유기 염기의 존재하에, 실온에서 반응 혼합물의 비점까지의 온도 범위에서, 하기식(II)의 피리다지논을 식(III)의 화합물과 반응시키는 것을 특징으로 하는, 제1항에서 청구한 식(I)의 피리다지논의 제조방법.[상기식에서, R,X,Y,R1,R2,R3,R4,Z,Y1,W,Rx,R′,b,y,w 및 n은 제1항의 식(I)에서 정의한 바와같고; X′ 및 X″는 CL, Br 또는 I원자, 혹은 YH기(여기에서, Y는 상기 정의한 바와같다)를 나타내지만, 이들 중 어느 하나는 YH기로 구성되어야 하며, 다른 하나는 Cl, Br, 또는 I로 구성되어야 한다.]
- 제1항에서 청구한 식(I)의 피리다지논 1종 이상을 유효량으로 농작물, 원예작물, 및/또는 인간 및/또는 가축 및/또는 사육동물이 기거하는 공간에 사용함을 특징으로 하는, 농작물, 원예작물 및/또는 기거공간에 있어서 해충 및/또는 진드기의 침투 억제 방법.
- 제1항에서 청구한 식(I)의 피리다지논 1종 이상과 1종 이상의 고상 또는 액상 담체, 살충·살비제 분야에서 유용한 기타 첨가제 및/또는 다른 활성물질 및 비료를 함유하는 것을 특징으로 하는, 해충 및/또는 진드기 침투 억제용조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT8920013A IT1229684B (it) | 1989-04-05 | 1989-04-05 | Piridazinoni ad attivita' insetticida ed acaricida |
IT20013A/89 | 1989-04-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900016149A true KR900016149A (ko) | 1990-11-12 |
KR0140208B1 KR0140208B1 (ko) | 1998-06-01 |
Family
ID=11163119
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900004666A KR0140208B1 (ko) | 1989-04-05 | 1990-04-04 | 살충, 살비활성의 피리다지논 |
Country Status (9)
Country | Link |
---|---|
US (1) | US5169848A (ko) |
EP (1) | EP0391390B1 (ko) |
JP (1) | JP2807035B2 (ko) |
KR (1) | KR0140208B1 (ko) |
AT (1) | ATE118210T1 (ko) |
CA (1) | CA2013687A1 (ko) |
DE (1) | DE69016687T2 (ko) |
ES (1) | ES2068935T3 (ko) |
IT (1) | IT1229684B (ko) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02279676A (ja) * | 1989-04-19 | 1990-11-15 | Otsuka Chem Co Ltd | ピリダジノン誘導体 |
US5286725A (en) * | 1990-09-17 | 1994-02-15 | Ministero Dell'universita' E Della Ricerca Scientifica E Technologica | Pyridazinones endowed with acaricide and insecticide action |
US5312990A (en) * | 1993-05-28 | 1994-05-17 | Hoechst Celanese Corporation | Di-amino compounds |
US5300691A (en) * | 1993-05-28 | 1994-04-05 | Hoechst Celanese Corporation | Substituted benzyl amines |
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JP2001335565A (ja) * | 2000-05-31 | 2001-12-04 | Mitsubishi Chemicals Corp | ピリダジノン類およびこれを有効成分とする有害生物防除剤 |
JP4640538B2 (ja) * | 2000-06-27 | 2011-03-02 | 日本農薬株式会社 | ピリダジノン類およびこれを有効成分とする有害生物防除剤 |
US7344702B2 (en) | 2004-02-13 | 2008-03-18 | Bristol-Myers Squibb Pharma Company | Contrast agents for myocardial perfusion imaging |
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US7824659B2 (en) | 2005-08-10 | 2010-11-02 | Lantheus Medical Imaging, Inc. | Methods of making radiolabeled tracers and precursors thereof |
PT2257315T (pt) | 2008-02-29 | 2020-01-27 | Lantheus Medical Imaging Inc | Agentes de contraste para aplicações incluindo imagiologia de perfusão |
WO2010057691A2 (en) * | 2008-08-11 | 2010-05-27 | Solvay Solexis S.P.A. | Hydrofluoroalcohols with improved thermal and chemical stability |
CA2758883C (en) | 2009-04-15 | 2020-03-10 | Lantheus Medical Imaging, Inc. | Stabilization of radiopharmaceutical compositions using ascorbic acid |
EP2534136B1 (en) | 2010-02-08 | 2017-09-06 | Lantheus Medical Imaging, Inc. | Methods for synthesizing imaging agents, and intermediates thereof |
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Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4571397A (en) * | 1982-03-05 | 1986-02-18 | Nissan Chemical Industries | Pyridazinone derivatives, preparation thereof, and agricultural and horticultural fungicidal, insecticidal, acaricidal, nematicidal compositions containing said derivatives |
GR79933B (ko) * | 1983-06-23 | 1984-10-31 | Nissan Chemical Ind Ltd | |
EP0183212B1 (en) * | 1984-11-29 | 1990-06-20 | Nissan Chemical Industries Ltd. | Pyridazinone derivatives, preparation thereof, and insecticidal, acaricidal, nematicidal, fungicidal compositions |
US4837217A (en) * | 1985-04-19 | 1989-06-06 | Nissan Chemical Industries, Ltd. | Pyridazinone derivatives, preparation thereof, and insecticidal, acaricidal, nematicidal, fungicidal compositions |
YU134686A (en) * | 1985-07-30 | 1988-02-29 | Nissan Chemical Ind Ltd | Process for preparing new derivatives 3-(2h)-pyridazinone |
ZA87704B (en) * | 1986-02-08 | 1987-09-30 | Nissan Chemical Ind Ltd | Pyridazinone derivatives,preparation thereof,and insecticidal,acaricidal,nematicidal,fungicidal compositions |
EP0283271A3 (en) * | 1987-03-17 | 1990-04-25 | Ube Industries, Ltd. | Pyridazinone derivative, process for producing thereof and insecticide, acaricide and fungicide containing said derivative as active ingredient |
JPS63275569A (ja) * | 1987-05-07 | 1988-11-14 | Nissan Chem Ind Ltd | ピリダジノン誘導体および害虫防除剤 |
JPH0638630B2 (ja) * | 1987-07-13 | 1994-05-18 | 株式会社日立製作所 | マルチスキャン水平発振回路 |
JPH01112057A (ja) * | 1987-10-23 | 1989-04-28 | Japan Autom Transmission Co Ltd | 副変速機付多段自動変速機 |
-
1989
- 1989-04-05 IT IT8920013A patent/IT1229684B/it active
-
1990
- 1990-04-03 CA CA002013687A patent/CA2013687A1/en not_active Abandoned
- 1990-04-04 ES ES90106436T patent/ES2068935T3/es not_active Expired - Lifetime
- 1990-04-04 DE DE69016687T patent/DE69016687T2/de not_active Expired - Fee Related
- 1990-04-04 AT AT90106436T patent/ATE118210T1/de not_active IP Right Cessation
- 1990-04-04 EP EP90106436A patent/EP0391390B1/en not_active Expired - Lifetime
- 1990-04-04 KR KR1019900004666A patent/KR0140208B1/ko not_active IP Right Cessation
- 1990-04-04 US US07/504,020 patent/US5169848A/en not_active Expired - Fee Related
- 1990-04-05 JP JP2091336A patent/JP2807035B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0391390A1 (en) | 1990-10-10 |
CA2013687A1 (en) | 1990-10-05 |
IT1229684B (it) | 1991-09-06 |
IT8920013A0 (it) | 1989-04-05 |
ES2068935T3 (es) | 1995-05-01 |
KR0140208B1 (ko) | 1998-06-01 |
DE69016687T2 (de) | 1995-06-08 |
US5169848A (en) | 1992-12-08 |
EP0391390B1 (en) | 1995-02-08 |
DE69016687D1 (de) | 1995-03-23 |
ATE118210T1 (de) | 1995-02-15 |
JPH0356466A (ja) | 1991-03-12 |
JP2807035B2 (ja) | 1998-09-30 |
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