NO313458B1 - Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter - Google Patents
Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter Download PDFInfo
- Publication number
- NO313458B1 NO313458B1 NO19993107A NO993107A NO313458B1 NO 313458 B1 NO313458 B1 NO 313458B1 NO 19993107 A NO19993107 A NO 19993107A NO 993107 A NO993107 A NO 993107A NO 313458 B1 NO313458 B1 NO 313458B1
- Authority
- NO
- Norway
- Prior art keywords
- acetyl
- dichloro
- trifluoromethylphenyl
- methylsulfinylpyrazole
- amino
- Prior art date
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- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3388796P | 1996-12-24 | 1996-12-24 | |
PCT/EP1997/007115 WO1998028277A1 (en) | 1996-12-24 | 1997-12-18 | Pesticidal 1-arylpyrazoles |
Publications (3)
Publication Number | Publication Date |
---|---|
NO993107D0 NO993107D0 (no) | 1999-06-22 |
NO993107L NO993107L (no) | 1999-08-24 |
NO313458B1 true NO313458B1 (no) | 2002-10-07 |
Family
ID=21873039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19993107A NO313458B1 (no) | 1996-12-24 | 1999-06-22 | Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter |
Country Status (38)
Country | Link |
---|---|
US (2) | US6087387A (de) |
EP (1) | EP0948486B1 (de) |
JP (1) | JP2001506664A (de) |
KR (1) | KR20000062319A (de) |
CN (1) | CN1099415C (de) |
AP (1) | AP1237A (de) |
AR (1) | AR011048A1 (de) |
AU (1) | AU746514B2 (de) |
BG (1) | BG64857B1 (de) |
BR (1) | BR9714181A (de) |
CA (1) | CA2275635C (de) |
CO (1) | CO5031287A1 (de) |
CU (1) | CU22869A3 (de) |
CZ (1) | CZ294766B6 (de) |
DE (1) | DE69738328T2 (de) |
DK (1) | DK0948486T3 (de) |
EA (1) | EA002085B1 (de) |
EE (1) | EE05495B1 (de) |
EG (1) | EG21715A (de) |
ES (1) | ES2297867T3 (de) |
HK (1) | HK1024476A1 (de) |
HR (1) | HRP970703B1 (de) |
HU (1) | HU229905B1 (de) |
ID (1) | ID19248A (de) |
IL (1) | IL130533A (de) |
MA (1) | MA24432A1 (de) |
MY (1) | MY128485A (de) |
NO (1) | NO313458B1 (de) |
NZ (1) | NZ336418A (de) |
OA (1) | OA11133A (de) |
PL (1) | PL193231B1 (de) |
PT (1) | PT948486E (de) |
RS (1) | RS49966B (de) |
SK (1) | SK285866B6 (de) |
TR (1) | TR199901473T2 (de) |
TW (1) | TW505503B (de) |
WO (1) | WO1998028277A1 (de) |
ZA (1) | ZA9711590B (de) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ294766B6 (cs) | 1996-12-24 | 2005-03-16 | Rhone-Poulenc Agro | 1-Arylpyrazolové sloučeniny, pesticidní prostředky obsahující tyto sloučeniny jako účinné látky a způsob hubení škůdců |
US6531501B1 (en) | 1998-12-11 | 2003-03-11 | Aventis Cropscience, S.A. | Control of arthropods in animals |
AR021608A1 (es) * | 1998-12-11 | 2002-07-31 | Merial Ltd | Represion de artropodos en animales |
MY129771A (en) | 1999-12-02 | 2007-04-30 | Merial Ltd | Control of arthropods in animals |
BR0111654A (pt) * | 2000-06-09 | 2003-05-20 | Bayer Cropscience Sa | Processo de preparação de compostos pesticidas |
EP1483245B1 (de) * | 2002-03-05 | 2006-08-09 | Bayer CropScience S.A. | 5-substituierte alkylaminopyrazol-derivate als pestizide |
WO2006045522A1 (en) * | 2004-10-22 | 2006-05-04 | Basf Aktiengesellschaft | Pesticidal mixtures |
WO2006050772A1 (en) * | 2004-11-11 | 2006-05-18 | Merial Ltd. | Vinylaminopyrazole derivatives as pesticides |
AU2006327317B2 (en) * | 2005-12-23 | 2010-11-25 | Astrazeneca Ab | GABA-B receptor modulators |
CN101506150B (zh) | 2006-06-22 | 2013-08-28 | 巴斯夫欧洲公司 | 丙二腈化合物 |
AU2012203942B2 (en) * | 2006-07-05 | 2014-11-27 | Boehringer Ingelheim Animal Health USA Inc. | 1-aryl-5-alkyl pyrazole derivative compounds, processes of making and methods of using thereof |
CN101511795B (zh) * | 2006-07-05 | 2013-09-18 | 安万特农业公司 | 1-芳基-5-烷基吡唑衍生化合物、其制备方法和使用方法 |
TW200824563A (en) | 2006-09-14 | 2008-06-16 | Basf Ag | Pesticide composition |
JP2010509275A (ja) | 2006-11-10 | 2010-03-25 | ビーエーエスエフ ソシエタス・ヨーロピア | フィプロニルの結晶変態 |
SI2083629T2 (sl) | 2006-11-10 | 2015-03-31 | Basf Se | Kristalna modifikacija fipronila |
UA110598C2 (uk) | 2006-11-10 | 2016-01-25 | Басф Се | Спосіб одержання кристалічної модифікації фіпронілу |
US8188136B2 (en) | 2006-11-10 | 2012-05-29 | Basf Se | Crystalline modification of fipronil |
US9006142B2 (en) | 2006-11-30 | 2015-04-14 | Basf Se | Agrochemical formulations comprising 1-vinyl-2-pyrrolidinone co-polymers |
JP5323714B2 (ja) | 2006-11-30 | 2013-10-23 | ビーエーエスエフ ソシエタス・ヨーロピア | N−ビニルアミドコポリマーを含む農薬製剤 |
WO2008065050A1 (en) | 2006-11-30 | 2008-06-05 | Basf Se | Agrochemical formulations comprising co-polymers based on diisocyanates |
WO2008071714A1 (en) | 2006-12-15 | 2008-06-19 | Rohm And Haas Company | Mixtures comprising 1-methylcyclopropene |
DE102006061537A1 (de) * | 2006-12-27 | 2008-07-03 | Bayer Healthcare Ag | Mittel zur Bekämpfung von Parasiten an Tieren |
DE102006061538A1 (de) * | 2006-12-27 | 2008-07-03 | Bayer Healthcare Ag | Kombinationsprodukt zur Bekämpfung von Parasiten an Tieren |
BRPI0806347A2 (pt) | 2007-01-19 | 2011-09-06 | Basf Se | misturas fungicidas, agente fungicida, método para combater fungos nocivos fitopagênicos, semente, e, processo para preparar um agente |
CN101589030A (zh) | 2007-01-26 | 2009-11-25 | 巴斯夫欧洲公司 | 用于对抗动物害虫的3-氨基-1,2-苯并异噻唑化合物ⅱ |
EP1952690A3 (de) | 2007-01-31 | 2009-04-22 | Basf Se | Auf Triazolpyrimidinen und Insektiziden basierende pestizide Mischungen |
EP2679096A1 (de) | 2007-02-06 | 2014-01-01 | Basf Se | Pestizidgemische |
CN108402068B (zh) | 2007-04-12 | 2021-12-03 | 巴斯夫欧洲公司 | 包含氰基亚磺酰亚胺基化合物的农药混合物 |
CN101668860B (zh) | 2007-04-23 | 2014-02-12 | 巴斯夫欧洲公司 | 组合化学剂和转基因修饰增强植物生产力 |
CL2008002420A1 (es) | 2007-08-16 | 2009-10-23 | Basf Se | Uso de una composicion que comprende a) un ingrediente activo seleccionado de piraclostrobina; b) un sulfato de eter poliarilfenol polialcoxi; y c) un co-polimero basado en esteres metaacrilicos para el tratamiento de semillas y composicion para el tratamiento de semillas. |
JP2010536735A (ja) * | 2007-08-17 | 2010-12-02 | ビーエーエスエフ ソシエタス・ヨーロピア | 収穫量を増大させるための殺虫剤 |
BRPI0816948B1 (pt) | 2007-09-20 | 2018-01-23 | Basf Se | Composição fungicida, seus usos, agente fungicida, método para controlar fungos nocivos fitopatogênicos, e semente resistente a fungos nocivos fitopatogênicos |
BRPI0906577A2 (pt) | 2008-01-25 | 2019-09-24 | Syngenta Partcipations Ag | compostos químicos |
AU2009316899B2 (en) | 2008-11-19 | 2015-08-20 | Boehringer Ingelheim Animal Health USA Inc. | Compositions comprising 1-arylpyrazole alone or in combination with formamidine for the treatment of parasitic infection |
US9173728B2 (en) | 2008-11-19 | 2015-11-03 | Merial Inc. | Multi-cavity container having offset indentures for dispensing fluids |
EP2381769A2 (de) | 2008-12-23 | 2011-11-02 | Basf Se | Verfahren und wässrige formulierung zum imprägnieren von nichtlebenden materialien, das eine schutzwirkung gegen schädlinge vermittelt |
ES2472918T3 (es) | 2009-07-06 | 2014-07-03 | Basf Se | Compuestos de piridazina para controlar plagas de invertebrados |
WO2011117286A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2013000572A1 (de) | 2011-06-30 | 2013-01-03 | 2LUTION GmbH | Mittel zur bekämpfung von parasiten an tieren |
JO3626B1 (ar) | 2012-02-23 | 2020-08-27 | Merial Inc | تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها |
CN104370818B (zh) * | 2014-11-10 | 2017-04-05 | 浙江海正化工股份有限公司 | 一种氧化法制备乙虫腈的工艺 |
CN106866537A (zh) * | 2017-04-19 | 2017-06-20 | 江苏托球农化股份有限公司 | 一种乙虫腈的生产工艺 |
CN109651343B (zh) * | 2019-01-07 | 2020-06-19 | 中南民族大学 | 一种氟虫腈吡唑醇环酰亚胺化合物及其微波水热法方法与应用 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3602728A1 (de) * | 1985-05-17 | 1986-11-20 | Bayer Ag, 51373 Leverkusen | Schaedlingsbekaempfungsmittel auf basis von pyrazolderivaten |
US5232940A (en) * | 1985-12-20 | 1993-08-03 | Hatton Leslie R | Derivatives of N-phenylpyrazoles |
GB8531485D0 (en) * | 1985-12-20 | 1986-02-05 | May & Baker Ltd | Compositions of matter |
GB8713768D0 (en) * | 1987-06-12 | 1987-07-15 | May & Baker Ltd | Compositions of matter |
US4918085A (en) * | 1989-03-02 | 1990-04-17 | Rhone-Poulenc Ag Company | Pesticidal 3-cyano-5-alkoxy-1-arylpyrazoles, compositions and use |
YU47834B (sr) * | 1989-08-10 | 1996-01-09 | Schering Agrochemical Limited | Azolni pesticid |
AU655014B2 (en) * | 1991-04-30 | 1994-12-01 | Merial Limited | Pesticidal 1-aryl-5-(substituted alkylideneimino)-pyrazoles |
GB9120641D0 (en) * | 1991-09-27 | 1991-11-06 | Ici Plc | Heterocyclic compounds |
ATE200985T1 (de) * | 1993-01-25 | 2001-05-15 | Sonus Pharma Inc | Phase-stift kolloide zur verwendung als ultraschallkontrastmittel |
GB9306184D0 (en) * | 1993-03-25 | 1993-05-19 | Zeneca Ltd | Heteroaromatic compounds |
JP3559849B2 (ja) * | 1993-07-30 | 2004-09-02 | アイエムシーオーアール ファーマシューティカル カンパニー | 超音波技術のための安定化された微小気泡組成物 |
US5798091A (en) * | 1993-07-30 | 1998-08-25 | Alliance Pharmaceutical Corp. | Stabilized gas emulsion containing phospholipid for ultrasound contrast enhancement |
DE4343832A1 (de) * | 1993-12-22 | 1995-06-29 | Bayer Ag | Substituierte 1-Arylpyrazole |
DE19511269A1 (de) * | 1994-03-30 | 1995-10-05 | Ciba Geigy Ag | Pyrazole |
DE4414333A1 (de) * | 1994-04-25 | 1995-10-26 | Bayer Ag | Substituierte Pyridylpyrazole |
EP0822187A4 (de) * | 1995-02-07 | 1998-05-13 | Nissan Chemical Ind Ltd | Pyrazolderivate als herbizide |
DE19518054A1 (de) * | 1995-03-08 | 1996-09-12 | Hoechst Schering Agrevo Gmbh | N-Arylpyrazolketone und deren Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
EP0780378B1 (de) * | 1995-12-19 | 2003-04-09 | Bayer CropScience S.A. | Neue 1-Aryl Pyrazol Derivate und ihre Verwendung als Schädlingsbekämpfungsmittel |
CZ294766B6 (cs) | 1996-12-24 | 2005-03-16 | Rhone-Poulenc Agro | 1-Arylpyrazolové sloučeniny, pesticidní prostředky obsahující tyto sloučeniny jako účinné látky a způsob hubení škůdců |
-
1997
- 1997-12-18 CZ CZ19992298A patent/CZ294766B6/cs not_active IP Right Cessation
- 1997-12-18 AU AU58575/98A patent/AU746514B2/en not_active Expired
- 1997-12-18 KR KR1019997005758A patent/KR20000062319A/ko not_active IP Right Cessation
- 1997-12-18 AP APAP/P/1999/001588A patent/AP1237A/en active
- 1997-12-18 PL PL334236A patent/PL193231B1/pl unknown
- 1997-12-18 PT PT97954422T patent/PT948486E/pt unknown
- 1997-12-18 WO PCT/EP1997/007115 patent/WO1998028277A1/en active IP Right Grant
- 1997-12-18 HU HU0000583A patent/HU229905B1/hu unknown
- 1997-12-18 NZ NZ336418A patent/NZ336418A/en not_active IP Right Cessation
- 1997-12-18 EA EA199900592A patent/EA002085B1/ru not_active IP Right Cessation
- 1997-12-18 CN CN97180938A patent/CN1099415C/zh not_active Expired - Lifetime
- 1997-12-18 DE DE69738328T patent/DE69738328T2/de not_active Expired - Lifetime
- 1997-12-18 DK DK97954422T patent/DK0948486T3/da active
- 1997-12-18 EE EEP199900321A patent/EE05495B1/xx unknown
- 1997-12-18 EP EP97954422A patent/EP0948486B1/de not_active Expired - Lifetime
- 1997-12-18 RS YUP-295/99A patent/RS49966B/sr unknown
- 1997-12-18 CA CA002275635A patent/CA2275635C/en not_active Expired - Lifetime
- 1997-12-18 IL IL13053397A patent/IL130533A/xx not_active IP Right Cessation
- 1997-12-18 SK SK857-99A patent/SK285866B6/sk not_active IP Right Cessation
- 1997-12-18 JP JP52835098A patent/JP2001506664A/ja active Pending
- 1997-12-18 TR TR1999/01473T patent/TR199901473T2/xx unknown
- 1997-12-18 ES ES97954422T patent/ES2297867T3/es not_active Expired - Lifetime
- 1997-12-18 BR BR9714181-0A patent/BR9714181A/pt not_active Application Discontinuation
- 1997-12-22 HR HR970703A patent/HRP970703B1/xx not_active IP Right Cessation
- 1997-12-23 MA MA24912A patent/MA24432A1/fr unknown
- 1997-12-23 AR ARP970106146A patent/AR011048A1/es unknown
- 1997-12-23 MY MYPI97006260A patent/MY128485A/en unknown
- 1997-12-23 ZA ZA9711590A patent/ZA9711590B/xx unknown
- 1997-12-23 CO CO97074746A patent/CO5031287A1/es unknown
- 1997-12-24 ID IDP973973A patent/ID19248A/id unknown
- 1997-12-24 EG EG139097A patent/EG21715A/xx active
-
1998
- 1998-03-02 TW TW086119718A patent/TW505503B/zh not_active IP Right Cessation
-
1999
- 1999-06-22 NO NO19993107A patent/NO313458B1/no not_active IP Right Cessation
- 1999-06-22 CU CU1999080A patent/CU22869A3/es unknown
- 1999-06-24 US US09/339,175 patent/US6087387A/en not_active Expired - Lifetime
- 1999-06-24 OA OA9900142A patent/OA11133A/en unknown
- 1999-07-19 BG BG103590A patent/BG64857B1/bg unknown
-
2000
- 2000-05-26 US US09/578,859 patent/US6403628B1/en not_active Expired - Lifetime
- 2000-06-23 HK HK00103819A patent/HK1024476A1/xx not_active IP Right Cessation
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MK1K | Patent expired |