TWI310300B - Active compound combinations having insecticidal and acaricidal properties - Google Patents
Active compound combinations having insecticidal and acaricidal properties Download PDFInfo
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- TWI310300B TWI310300B TW090102993A TW90102993A TWI310300B TW I310300 B TWI310300 B TW I310300B TW 090102993 A TW090102993 A TW 090102993A TW 90102993 A TW90102993 A TW 90102993A TW I310300 B TWI310300 B TW I310300B
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- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 1
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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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10007411A DE10007411A1 (de) | 2000-02-18 | 2000-02-18 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
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| TWI310300B true TWI310300B (en) | 2009-06-01 |
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| TW090102993A TWI310300B (en) | 2000-02-18 | 2001-02-12 | Active compound combinations having insecticidal and acaricidal properties |
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| JP (1) | JP4928700B2 (enExample) |
| KR (1) | KR100740977B1 (enExample) |
| CN (1) | CN1262187C (enExample) |
| AR (1) | AR031553A1 (enExample) |
| AT (1) | ATE301931T1 (enExample) |
| AU (1) | AU775704B2 (enExample) |
| BR (1) | BR0108427B1 (enExample) |
| CA (1) | CA2400425C (enExample) |
| CO (1) | CO5231190A1 (enExample) |
| DE (2) | DE10007411A1 (enExample) |
| EG (1) | EG22825A (enExample) |
| ES (1) | ES2244581T3 (enExample) |
| GT (1) | GT200100024A (enExample) |
| HN (1) | HN2001000025A (enExample) |
| HU (1) | HUP0204343A3 (enExample) |
| IL (2) | IL151068A0 (enExample) |
| MX (1) | MXPA02008011A (enExample) |
| PL (1) | PL356369A1 (enExample) |
| SV (1) | SV2002000315A (enExample) |
| TW (1) | TWI310300B (enExample) |
| WO (1) | WO2001060158A1 (enExample) |
| ZA (1) | ZA200205784B (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10007411A1 (de) * | 2000-02-18 | 2001-08-23 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10013914A1 (de) * | 2000-03-21 | 2001-09-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10015310A1 (de) * | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10017881A1 (de) * | 2000-04-11 | 2001-10-25 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10018370A1 (de) * | 2000-04-14 | 2001-10-18 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| AU2007101011B9 (en) * | 2002-12-05 | 2008-04-17 | Osmose (Australia) Pty Limited | Superficial Treatment for Wood and Wood Products |
| AU2002953128A0 (en) * | 2002-12-05 | 2002-12-19 | Osmose (Australia) Pty Ltd | Surface treatment for wood and wood products |
| US8637089B2 (en) | 2003-04-09 | 2014-01-28 | Osmose, Inc. | Micronized wood preservative formulations |
| KR101110669B1 (ko) | 2003-04-09 | 2012-02-17 | 오스모스 인코포레이티드 | 미세화된 목재 방부제 제형 |
| US8701743B2 (en) | 2004-01-02 | 2014-04-22 | Water Gremlin Company | Battery parts and associated systems and methods |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| DE102006008691A1 (de) * | 2006-02-24 | 2007-08-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EP2083632A2 (en) * | 2006-11-21 | 2009-08-05 | Mitam Ltd. | Formulations of entomopathogenic fungi for insect control |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| WO2010036882A1 (en) * | 2008-09-29 | 2010-04-01 | The Hartz Mountain Corporation | Photo-stable pest control |
| ES2746292T3 (es) | 2009-04-30 | 2020-03-05 | Water Gremlin Co | Piezas de bateria que tienen elementos de retención y sellado |
| US20110129574A1 (en) * | 2009-11-30 | 2011-06-02 | Pathak Chandrashekhar P | Methods and compositions for filling fleshy fruits and vegetables |
| CN102811617A (zh) * | 2010-01-22 | 2012-12-05 | 拜耳知识产权有限责任公司 | 杀螨和/或杀虫活性物质结合物 |
| WO2011144742A1 (en) | 2010-05-21 | 2011-11-24 | Chemilia Ab | Novel pyrimidine derivatives |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
| US9748551B2 (en) | 2011-06-29 | 2017-08-29 | Water Gremlin Company | Battery parts having retaining and sealing features and associated methods of manufacture and use |
| CN103621548B (zh) * | 2012-08-28 | 2015-10-28 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与拟除虫菊酯类的杀虫组合物 |
| CN103621509B (zh) * | 2012-08-28 | 2015-10-21 | 陕西美邦农药有限公司 | 一种含螺甲螨酯的农药组合物 |
| CN103621503B (zh) * | 2012-08-29 | 2016-01-13 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与双酰肼类的农药组合物 |
| US9954214B2 (en) | 2013-03-15 | 2018-04-24 | Water Gremlin Company | Systems and methods for manufacturing battery parts |
| CN105766910A (zh) * | 2016-03-31 | 2016-07-20 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和杀虫双的杀虫组合物 |
| CN105746570A (zh) * | 2016-03-31 | 2016-07-13 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和四氟苯菊酯的杀虫组合物 |
| CN105831118A (zh) * | 2016-03-31 | 2016-08-10 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和杀虫环的杀虫组合物 |
| CN108976215B (zh) * | 2017-05-31 | 2022-02-11 | 河北兰升生物科技有限公司 | 苯基酮烯醇衍生物的晶体及其制备方法、以及包含该晶体的农药组合物 |
Family Cites Families (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US403680A (en) * | 1889-05-21 | Hinge-screw coupling for fishing-net frames | ||
| US462237A (en) * | 1891-11-03 | Electric-lighting system | ||
| US3264177A (en) | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
| GB1168797A (en) | 1965-12-09 | 1969-10-29 | Nat Res Dev | Cyclopropane Carboxylic Acid Derivatives and their use as Insecticides |
| JPS515450B1 (enExample) | 1971-06-29 | 1976-02-20 | ||
| US4622337A (en) | 1972-05-25 | 1986-11-11 | National Research Development Corporation | 2,2-dimethyl-3-(2-halovinyl)cyclopropane carboxlic acid ester pesticides |
| US4024163A (en) | 1972-05-25 | 1977-05-17 | National Research Development Corporation | Insecticides |
| DE2326077C2 (de) | 1972-05-25 | 1985-12-12 | National Research Development Corp., London | Ungesättigte Cyclopropancarbonsäuren und deren Derivate, deren Herstellung und diese enthaltende Insektizide |
| US4039680A (en) | 1972-07-11 | 1977-08-02 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| US4062968A (en) | 1972-07-11 | 1977-12-13 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| US4031235A (en) | 1972-07-11 | 1977-06-21 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| US4016179A (en) | 1972-07-11 | 1977-04-05 | Sumitomo Chemical Co | Certain esters of 2-substituted-4-hydroxy-cyclopent-2-enones |
| EG11383A (en) | 1972-07-11 | 1979-03-31 | Sumitomo Chemical Co | Novel composition for controlling nixious insects and process for preparing thereof |
| US4058622A (en) | 1972-07-11 | 1977-11-15 | Sumitomo Chemical Company, Limited | Substituted phenyl acetate, insecticidal composition and method of use |
| US4070481A (en) | 1975-09-15 | 1978-01-24 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4055661A (en) | 1974-12-11 | 1977-10-25 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4148918A (en) | 1974-05-10 | 1979-04-10 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4053634A (en) | 1975-09-15 | 1977-10-11 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4220591A (en) | 1975-11-26 | 1980-09-02 | Commonwealth Scientific And Industrial Research Organization | Insecticidal esters |
| SE7610038L (sv) | 1976-03-29 | 1977-09-20 | Du Pont | Miticida och aficida karboxylsyraestrar |
| JPS5324019A (en) | 1976-08-18 | 1978-03-06 | Sumitomo Chem Co Ltd | Inspecticide comprising optically active isomer of alpha-cyano-3-phenoxybenzyl-2-(4-chlorophenyl)-isovalerate as an effective component |
| SE441179B (sv) | 1976-09-21 | 1985-09-16 | Roussel Uclaf | Nya cyklopropankarboxylsyror med polyhalogenerad substituent, sett for framstellning derav samt anvendning derav i pesticidkompositioner |
| IL56400A (en) | 1976-09-21 | 1984-07-31 | Roussel Uclaf | Alpha-cyano-3-phenoxybenzyl and 3,4,5,6-tetrahydrophthalimidomethyl esters of 2,2-dimethyl-3-(1,2,2,2-tetrahaloethyl)cyclopropane-carboxylic acids,process for preparing them and insecticidal,acaricidal and nematocidal compositions containing them |
| US4239777A (en) | 1976-10-01 | 1980-12-16 | American Cyanamid Company | (-)-α-Cyano-m-phenoxybenzyl(+)-α-isopropyl-4-difluoromethoxyphenylacetate |
| US4178460A (en) | 1976-10-01 | 1979-12-11 | American Cyanamid Co. | 2-Haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)-phenylalkanoic acids |
| US4199595A (en) | 1976-10-01 | 1980-04-22 | American Cyanamid Company | M-phenoxybenzyl and α-cyano-M-phenoxybenzyl esters of 2-haloalkyl (oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids |
| US4330675A (en) | 1977-01-24 | 1982-05-18 | Imperial Chemical Industries Limited | Halogenated esters |
| US4183948A (en) | 1977-01-24 | 1980-01-15 | Imperial Chemical Industries Limited | Halogenated esters |
| US4378316A (en) | 1977-01-24 | 1983-03-29 | Imperial Chemical Industries Limited | Halogenated esters |
| DE2709264C3 (de) | 1977-03-03 | 1982-01-21 | Bayer Ag, 5090 Leverkusen | Substituierte Phenoxybenzyloxycarbonylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide sowie neue Zwischenprodukte |
| US4143157A (en) | 1977-08-25 | 1979-03-06 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1'4-naphthoquinone carboxylic acid esters |
| US4329518A (en) | 1979-09-18 | 1982-05-11 | Fmc Corporation | Insecticidal [1,1'-biphenyl]-3-ylmethyl esters |
| US4668792A (en) | 1978-12-04 | 1987-05-26 | Fmc Corporation | Intermediates to insecticidal [1,1'-biphenyl]-3-ylmethyl esters |
| US4254052A (en) | 1979-09-27 | 1981-03-03 | Fmc Corporation | Preparation of esters |
| US4254051A (en) | 1979-09-27 | 1981-03-03 | Fmc Corporation | Preparation of esters |
| US4254050A (en) | 1979-09-27 | 1981-03-03 | Fmc Corporation | Preparation of esters |
| US4402973A (en) | 1980-10-02 | 1983-09-06 | Fmc Corporation | Insecticidal (1,1'-biphenyl)-3-ylmethyl esters |
| US4260633A (en) | 1980-04-21 | 1981-04-07 | Zoecon Corporation | Pesticidal esters of amino acids |
| US4397864A (en) | 1980-05-02 | 1983-08-09 | Mitsuitoatsu Chemicals Inc. | 2-Arylpropyl ether or thioether derivatives and insecticidal and acaricidal agents containing said derivatives |
| US4322534A (en) | 1980-06-06 | 1982-03-30 | Fmc Corporation | Preparation of esters |
| US4323685A (en) | 1980-06-13 | 1982-04-06 | Fmc Corporation | Preparation of esters |
| US4322535A (en) | 1980-06-13 | 1982-03-30 | Fmc Corporation | Preparation of esters |
| US4732903A (en) | 1980-07-02 | 1988-03-22 | Roussel Uclaf | Certain cyclopropyl dicarboxylates having pesticidal and insecticidal activity |
| US4536591A (en) | 1981-05-21 | 1985-08-20 | Fmc Corporation | Insecticidal [1,1'-biphenyl]-3-ylmethyl esters |
| GB8308507D0 (en) | 1983-03-28 | 1983-05-05 | Ici Plc | Insecticidal product |
| ZA836964B (en) | 1982-10-11 | 1984-05-30 | Ici Plc | Insecticidal product and preparation thereof |
| DE3522629A1 (de) | 1985-06-25 | 1987-01-08 | Bayer Ag | Verfahren zur herstellung bestimmter enantiomerenpaare von permethrinsaeure-(alpha)-cyano-3-phenoxy-4-fluor-benzyl -ester |
| IL79360A (en) | 1985-07-12 | 1993-02-21 | Ciba Geigy Ag | Aleyrodidae-controlling compositions containing n-(4-phenoxy-2,6- diisopropylphenyl) -n)-tert- butylthiourea as active agent |
| US4843068A (en) | 1985-12-27 | 1989-06-27 | Nihon Nohyaku Co., Ltd. | Pyrazole oxime derivatives and compositions |
| DE3604781A1 (de) | 1986-02-13 | 1987-08-27 | Schering Ag | Neue silane, verfahren zu ihrer herstellung und diese verbindungen enthaltende einsektizide mittel |
| US4782094A (en) | 1986-03-14 | 1988-11-01 | Mitsui Toatsu Chemicals, Inc. | Difluorobromomethoxyphenyl derivative and miticide comprising said derivative as active ingredient |
| US5310938A (en) | 1987-07-29 | 1994-05-10 | American Cyanamid Company | Substituted arylpyrrole compounds |
| US5010098A (en) | 1987-07-29 | 1991-04-23 | American Cyanamid Company | Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof |
| DE4216814A1 (de) * | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate |
| RU2109730C1 (ru) | 1991-11-22 | 1998-04-27 | Юнироял Кемикал Компани, Инк. | Фенилгидразиновые производные, способ борьбы с вредителями и инсектоакарицидонематоцидная композиция |
| EP0641316B1 (en) | 1991-11-22 | 1997-01-22 | UNIROYAL CHEMICAL COMPANY, Inc. | Insecticidal phenylhydrazine derivatives |
| EP0639572B1 (en) | 1992-04-28 | 1998-07-29 | Yashima Chemical Industry Co., Ltd. | 2-(2,6-difluorophenyl)-4-(2-ethoxy-4-tert-butylphenyl)-2-oxazoline |
| HUT73746A (en) | 1993-07-05 | 1996-09-30 | Bayer Ag | Substituted aryl-keto-enolic heterocycles, process for preparation the same and their use as arthropodes, fungicides and herbicides |
| ES2127859T3 (es) | 1993-09-17 | 1999-05-01 | Bayer Ag | Derivados de la 3-aril-4-hidroxi-3-dihidrofuranona. |
| WO1996016061A1 (de) | 1994-11-17 | 1996-05-30 | Bayer Aktiengesellschaft | Substituierte thiophenderivate als schädlingsbekämpfungsmittel und herbizide |
| EP0799228B1 (de) | 1994-12-23 | 2003-03-19 | Bayer CropScience AG | 3-aryl-tetronsäure-derivate, deren herstellung und deren verwendung als schädlingsbekämpfungsmittel |
| CN1154634C (zh) | 1995-02-13 | 2004-06-23 | 拜尔公司 | 作为除草剂和杀虫剂的2-苯基取代杂环1,3-酮烯醇 |
| CN1131209C (zh) | 1995-05-09 | 2003-12-17 | 拜尔公司 | 可用作杀虫剂和除草剂的烷基－二卤代苯基取代的酮烯醇 |
| ES2180786T3 (es) | 1995-06-28 | 2003-02-16 | Bayer Ag | Fenilcetoenoles 2,4,5-trisubstituidos para el empleo como pesticidas y herbicidas. |
| CN1152860C (zh) | 1995-06-30 | 2004-06-09 | 拜尔公司 | 二烷基-卤代苯基取代的酮-烯醇 |
| TR199801990T2 (xx) | 1996-04-02 | 2000-06-21 | Bayer Aktiengesellschaft | Yeni ikameli fenilketoenoller. |
| AU2773397A (en) | 1996-05-10 | 1997-12-05 | Bayer Aktiengesellschaft | New substituted pyridyl keto enols |
| US6114374A (en) | 1996-08-05 | 2000-09-05 | Bayer Aktiengesellschaft | 2-and 2,5-substituted phenylketoenols |
| DE19632126A1 (de) | 1996-08-09 | 1998-02-12 | Bayer Ag | Phenylsubstituierte cyclische Ketoenole |
| DE19742492A1 (de) | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
| DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19939395A1 (de) | 1998-10-23 | 2000-04-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE19913174A1 (de) * | 1999-03-24 | 2000-09-28 | Bayer Ag | Synergistische insektizide Mischungen |
| DE19953775A1 (de) * | 1999-11-09 | 2001-05-10 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10007411A1 (de) * | 2000-02-18 | 2001-08-23 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
-
2000
- 2000-02-18 DE DE10007411A patent/DE10007411A1/de not_active Withdrawn
-
2001
- 2001-01-14 EG EG20010129A patent/EG22825A/xx active
- 2001-01-30 AR ARP010100417A patent/AR031553A1/es active IP Right Grant
- 2001-02-06 MX MXPA02008011A patent/MXPA02008011A/es active IP Right Grant
- 2001-02-06 ES ES01902414T patent/ES2244581T3/es not_active Expired - Lifetime
- 2001-02-06 CN CNB018049605A patent/CN1262187C/zh not_active Expired - Lifetime
- 2001-02-06 KR KR1020027009781A patent/KR100740977B1/ko not_active Expired - Lifetime
- 2001-02-06 AU AU30249/01A patent/AU775704B2/en not_active Expired
- 2001-02-06 HU HU0204343A patent/HUP0204343A3/hu unknown
- 2001-02-06 PL PL01356369A patent/PL356369A1/xx not_active Application Discontinuation
- 2001-02-06 DE DE50107115T patent/DE50107115D1/de not_active Expired - Fee Related
- 2001-02-06 CA CA2400425A patent/CA2400425C/en not_active Expired - Fee Related
- 2001-02-06 AT AT01902414T patent/ATE301931T1/de not_active IP Right Cessation
- 2001-02-06 BR BRPI0108427-5A patent/BR0108427B1/pt not_active IP Right Cessation
- 2001-02-06 IL IL15106801A patent/IL151068A0/xx active IP Right Grant
- 2001-02-06 US US10/204,011 patent/US6653343B2/en not_active Expired - Lifetime
- 2001-02-06 EP EP01902414A patent/EP1263287B1/de not_active Expired - Lifetime
- 2001-02-06 JP JP2001559265A patent/JP4928700B2/ja not_active Expired - Lifetime
- 2001-02-06 WO PCT/EP2001/001237 patent/WO2001060158A1/de not_active Ceased
- 2001-02-07 GT GT200100024A patent/GT200100024A/es unknown
- 2001-02-12 TW TW090102993A patent/TWI310300B/zh not_active IP Right Cessation
- 2001-02-15 HN HN2001000025A patent/HN2001000025A/es unknown
- 2001-02-16 CO CO01012557A patent/CO5231190A1/es not_active Application Discontinuation
- 2001-02-16 SV SV2001000315A patent/SV2002000315A/es not_active Application Discontinuation
-
2002
- 2002-07-19 ZA ZA200205784A patent/ZA200205784B/en unknown
- 2002-08-05 IL IL151068A patent/IL151068A/en unknown
-
2003
- 2003-08-29 US US10/652,153 patent/US7091233B2/en not_active Expired - Lifetime
-
2006
- 2006-02-08 US US11/349,681 patent/US7232845B2/en not_active Expired - Lifetime
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| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |