CN1915023A - 具有杀虫和杀螨性能的活性化合物组合物 - Google Patents
具有杀虫和杀螨性能的活性化合物组合物 Download PDFInfo
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- CN1915023A CN1915023A CNA2006101059116A CN200610105911A CN1915023A CN 1915023 A CN1915023 A CN 1915023A CN A2006101059116 A CNA2006101059116 A CN A2006101059116A CN 200610105911 A CN200610105911 A CN 200610105911A CN 1915023 A CN1915023 A CN 1915023A
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- 238000004321 preservation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
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- 210000001938 protoplast Anatomy 0.000 description 1
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- 239000002728 pyrethroid Substances 0.000 description 1
- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
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- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
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- 239000010409 thin film Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
-
- 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
- A01N47/06—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 containing —O—CO—O— groups; Thio analogues 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/16—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof the nitrogen atom being part of a heterocyclic ring
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10043610.2 | 2000-09-05 | ||
| DE10043610A DE10043610A1 (de) | 2000-09-05 | 2000-09-05 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN01815123A Division CN1452457A (zh) | 2000-09-05 | 2001-08-23 | 具有杀虫和杀螨性能的活性化合物组合物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1915023A true CN1915023A (zh) | 2007-02-21 |
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Family Applications (2)
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|---|---|---|---|
| CNA2006101059116A Pending CN1915023A (zh) | 2000-09-05 | 2001-08-23 | 具有杀虫和杀螨性能的活性化合物组合物 |
| CN01815123A Pending CN1452457A (zh) | 2000-09-05 | 2001-08-23 | 具有杀虫和杀螨性能的活性化合物组合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN01815123A Pending CN1452457A (zh) | 2000-09-05 | 2001-08-23 | 具有杀虫和杀螨性能的活性化合物组合物 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7084138B2 (enExample) |
| EP (1) | EP1330161B1 (enExample) |
| JP (1) | JP2004508308A (enExample) |
| KR (1) | KR100745448B1 (enExample) |
| CN (2) | CN1915023A (enExample) |
| AR (1) | AR032472A1 (enExample) |
| AT (1) | ATE308884T1 (enExample) |
| AU (2) | AU8211901A (enExample) |
| BR (1) | BR0114043B1 (enExample) |
| CA (1) | CA2420874C (enExample) |
| DE (2) | DE10043610A1 (enExample) |
| ES (1) | ES2248378T3 (enExample) |
| IL (2) | IL154564A0 (enExample) |
| MX (1) | MXPA03001824A (enExample) |
| RU (1) | RU2287932C2 (enExample) |
| TW (1) | TWI278282B (enExample) |
| WO (1) | WO2002019824A1 (enExample) |
| ZA (1) | ZA200301774B (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE10024934A1 (de) * | 2000-05-19 | 2001-11-22 | Bayer Ag | Wirkstoffkombinationen mit insektiziden akariziden Eigenschaften |
| DE10055941A1 (de) * | 2000-11-10 | 2002-05-23 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| DE10354629A1 (de) | 2003-11-22 | 2005-06-30 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE10356550A1 (de) † | 2003-12-04 | 2005-07-07 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| MY142815A (en) * | 2004-02-19 | 2011-01-14 | Univ Florida | Use of molt-accelerating compounds, ecdysteroids, analogs thereof, and chitin synthesis inhibitors for controlling termites. |
| DE102004035133A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
| DE102005008033A1 (de) * | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006031978A1 (de) * | 2006-07-11 | 2008-01-17 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006031976A1 (de) * | 2006-07-11 | 2008-01-17 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006033154A1 (de) * | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EP1886564A1 (de) * | 2006-08-09 | 2008-02-13 | Bayer CropScience AG | Verwendung von Tetramsäurederivaten mit Düngern |
| EP2008519A1 (de) | 2007-06-28 | 2008-12-31 | Bayer CropScience AG | Verwendung von Wirkstoffkombinationen mit insektiziden Eigenschaften zur Bekämpfung von tierischen Schädlingen aus der Familie der Stinkwanzen |
| EP2011394A1 (de) * | 2007-07-03 | 2009-01-07 | Bayer CropScience AG | Verwendung von Tetramsäure - Derivaten zur Bekämpfung von virusübertragenden Vektoren |
| EP2039248A1 (de) * | 2007-09-21 | 2009-03-25 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| JP5563476B2 (ja) | 2007-12-20 | 2014-07-30 | バイエル・クロップサイエンス・アーゲー | 線虫類を防除するためのテトラミン酸誘導体の使用 |
| EP2127522A1 (de) * | 2008-05-29 | 2009-12-02 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| AU2009282194B2 (en) * | 2008-08-12 | 2012-04-19 | Dow Agrosciences Llc | Synergistic pesticidal compositions comprising an active compound, an ammonium salt, and a nonionic surfactant |
| US8683346B2 (en) * | 2008-11-17 | 2014-03-25 | Sap Portals Israel Ltd. | Client integration of information from a supplemental server into a portal |
| BRPI1007516A8 (pt) | 2009-01-29 | 2016-01-26 | Bayer Animal Health Gmbh | Dispositivo de controle pesticida de alto carregamento |
| DE102009028001A1 (de) | 2009-07-24 | 2011-01-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| WO2011100424A1 (en) * | 2010-02-12 | 2011-08-18 | Bayer Croscience Lp | Methods for reducing nematode damage to plants |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| CN102396472A (zh) * | 2011-11-26 | 2012-04-04 | 陕西美邦农药有限公司 | 一种含环氧虫啶和激素类的杀虫组合物 |
| CN102428949A (zh) * | 2011-12-21 | 2012-05-02 | 陕西美邦农药有限公司 | 一种含环氧虫啶和新烟碱类的杀虫组合物 |
| CN104222117A (zh) * | 2014-09-03 | 2014-12-24 | 扬州大学 | 含有螺虫乙酯的防治斑潜蝇和烟粉虱的农药制剂 |
| CN105994326A (zh) * | 2016-05-26 | 2016-10-12 | 深圳诺普信农化股份有限公司 | 一种含有螺虫乙酯的杀虫组合物 |
| CN106070220A (zh) * | 2016-05-31 | 2016-11-09 | 刘园 | 一种防治棉红蜘蛛的组合物及其制备方法 |
| CN111970929B (zh) * | 2018-04-13 | 2022-12-06 | 拜耳公司 | 具有杀昆虫、杀线虫和杀螨特性的活性成分结合物 |
Family Cites Families (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE537413A (enExample) | 1954-06-18 | |||
| US2758115A (en) | 1955-02-10 | 1956-08-07 | Bayer Ag | Derivatives of thiophosphoric acid |
| US3264177A (en) | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
| US3309266A (en) | 1965-07-01 | 1967-03-14 | Chevron Res | Insecticidal compositions containing oalkyl-s-alkyl phosphoroamidothioates and methods for killing insects therewith |
| GB1181657A (en) | 1966-03-31 | 1970-02-18 | Ici Ltd | Pyrimidine Derivatives and Compositions Containing them |
| US3933908A (en) | 1970-05-15 | 1976-01-20 | U.S. Philips Corporation | Substituted benzoyl ureas |
| US4110469A (en) * | 1970-05-15 | 1978-08-29 | U.S. Philips Corporation | Insecticidal N-(2,6-dichlorobenzoyl)-N'-(4-cyanophenyl) urea |
| US5342958A (en) * | 1970-05-15 | 1994-08-30 | Solvay Duphar International Research B.V. | Organic compounds derived from urea or thiourea |
| US5245071A (en) * | 1970-05-15 | 1993-09-14 | Duphar International Research B.V. | Organic compounds derived from urea or thiourea |
| US3989842A (en) | 1970-05-15 | 1976-11-02 | U.S. Philips Corporation | Certain substituted benzoyl urea insecticides |
| US4013717A (en) | 1970-05-15 | 1977-03-22 | U.S. Philips Corporation | Benzoyl phenyl urea derivatives having insecticidal activities |
| US4166124A (en) * | 1970-05-15 | 1979-08-28 | U.S. Philips Corporation | Insecticidal 2,6-dihalobenzoyl urea derivatives |
| NL160809C (nl) * | 1970-05-15 | 1979-12-17 | Duphar Int Res | Werkwijze ter bereiding van benzoylureumverbindingen, alsmede werkwijze ter bereiding van insekticide prepara- ten op basis van benzoylureumverbindingen. |
| 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 |
| 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 |
| 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 |
| 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 |
| US4097581A (en) * | 1975-12-12 | 1978-06-27 | Ciba-Geigy Corporation | Dioxolane derivatives |
| DE2601780B2 (de) * | 1976-01-20 | 1979-07-26 | Bayer Ag, 5090 Leverkusen | N-Phenyl-N'-benzoylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide |
| SE7610038L (sv) * | 1976-03-29 | 1977-09-20 | Du Pont | Miticida och aficida karboxylsyraestrar |
| CH604517A5 (enExample) | 1976-08-19 | 1978-09-15 | Ciba Geigy Ag | |
| 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 |
| NL189293C (nl) | 1978-02-06 | 1993-03-01 | Ishihara Sangyo Kaisha | Insecticide n-benzoyl-n'-fenylureumverbindingen en insecticide samenstelling op basis van een dergelijke verbinding. |
| CA1137506A (en) * | 1978-03-17 | 1982-12-14 | Ulf Fischer | Carbamic acid derivatives |
| EP0052833B1 (de) * | 1980-11-22 | 1983-12-14 | CELAMERCK GmbH & Co. KG | Harnstoffderivate, ihre Herstellung und Verwendung |
| US4468405A (en) * | 1981-07-30 | 1984-08-28 | The Dow Chemical Company | Substituted N-aroyl N'-phenyl urea compounds |
| US4427663A (en) * | 1982-03-16 | 1984-01-24 | Merck & Co., Inc. | 4"-Keto-and 4"-amino-4"-deoxy avermectin compounds and substituted amino derivatives thereof |
| CA1339745C (en) * | 1984-04-10 | 1998-03-17 | Martin Anderson | Pesticidal benzoylurea compounds |
| US4623658A (en) * | 1984-04-10 | 1986-11-18 | Shell Oil Company | Pesticidal benzoylurea compounds |
| EP0179022B1 (de) * | 1984-10-18 | 1990-11-07 | Ciba-Geigy Ag | Benzoylphenylharnstoffe |
| US5153224A (en) * | 1984-10-18 | 1992-10-06 | Ciba-Geigy Corporation | Benzoylphenylureas |
| IT1186717B (it) * | 1985-05-30 | 1987-12-16 | Donegani Guido Ist | Benzoil-uree ad attivita' insetticida |
| 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 |
| DE3683749D1 (de) | 1985-12-09 | 1992-03-12 | American Cyanamid Co | Insektentoetende diacylhydrazinverbindungen. |
| US5547974A (en) * | 1985-12-20 | 1996-08-20 | Rhone-Poulenc Agriculture Ltd. | Derivatives of N-phenylpyrazoles |
| US5232940A (en) * | 1985-12-20 | 1993-08-03 | Hatton Leslie R | Derivatives of N-phenylpyrazoles |
| US4843068A (en) * | 1985-12-27 | 1989-06-27 | Nihon Nohyaku Co., Ltd. | Pyrazole oxime derivatives and compositions |
| 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 |
| US5110986A (en) * | 1988-04-26 | 1992-05-05 | Rohm And Haas Company | Synthesis of n-t-alkyl-1,2-diacylhydrazines |
| DE3913682A1 (de) * | 1989-04-26 | 1990-10-31 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dione |
| US5142065A (en) | 1988-08-20 | 1992-08-25 | Bayer Aktiengesellschaft | 3-aryl-pyrrolidine-2,4-diones |
| US4985063A (en) * | 1988-08-20 | 1991-01-15 | Bayer Aktiengesellschaft | 3-aryl-pyrrolidine-2,4-diones |
| US5186737A (en) * | 1989-01-07 | 1993-02-16 | Bayer Aktiengesellschaft | Pesticidal 3-aryl-pyrrolidine-2,4-diones |
| DE3929087A1 (de) * | 1989-09-01 | 1991-03-07 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4032090A1 (de) * | 1990-02-13 | 1991-08-14 | Bayer Ag | Polycyclische 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4004496A1 (de) | 1990-02-14 | 1991-08-22 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4107394A1 (de) * | 1990-05-10 | 1991-11-14 | Bayer Ag | 1-h-3-aryl-pyrrolidin-2,4-dion-derivate |
| FR2665899B1 (fr) * | 1990-08-14 | 1994-04-01 | Roussel Uclaf | Nouveaux amides de l'acide [(aminocarbonyl) fluoromethyl] phosphonique, leur procede de preparation et leur application a la synthese de produits fluorocyanovinyliques. |
| US5462938A (en) * | 1990-12-21 | 1995-10-31 | Annus; Gary D. | Arthropodicidal oxadiazinyl, thiadiazinyl and triazinyl carboxanilides |
| IL100643A (en) * | 1991-01-25 | 1996-10-31 | Nippon Kayaku Kk | History of hydrazine and pesticides containing these histories as an active ingredient |
| DE4121365A1 (de) * | 1991-06-28 | 1993-01-14 | Bayer Ag | Substituierte 1-h-3-aryl-pyrrolidin-2,4-dion-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 |
| AU666040B2 (en) * | 1992-10-28 | 1996-01-25 | Bayer Aktiengesellschaft | Substituted 1-H-3-aryl-pyrrolidine-2,4-dione derivatives |
| DE4306259A1 (de) * | 1993-03-01 | 1994-09-08 | Bayer Ag | Dialkyl-1-H-3-(2,4-dimethylphenyl)-pyrrolidin-2,4-dione, ihre Herstellung und ihre Verwendung |
| DE4306257A1 (de) * | 1993-03-01 | 1994-09-08 | Bayer Ag | Substituierte 1-H-3-Phenyl-5-cycloalkylpyrrolidin-2,4-dione, ihre Herstellung und ihre Verwendung |
| 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 |
| ES2109613T3 (es) | 1993-08-19 | 1998-01-16 | Rohm & Haas | Preparacion de 1,2-diacil-2-(t-alquil)hidrazinas. |
| DE4425617A1 (de) * | 1994-01-28 | 1995-08-03 | Bayer Ag | 1-H-3-Aryl-pyrrolidin-2,4-dion-Derivate |
| DE4431730A1 (de) * | 1994-02-09 | 1995-08-10 | Bayer Ag | Substituierte 1H-3-Aryl-pyrrolidin-2,4-dion-Derivate |
| WO1995026954A1 (de) * | 1994-04-05 | 1995-10-12 | Bayer Aktiengesellschaft | Alkoxy-alkyl-substituierte 1-h-3-aryl-pyrrolidin-2,4-dione als herbizide und pestizide |
| 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 |
| KR100194534B1 (ko) * | 1996-06-29 | 1999-06-15 | 우종일 | 2-클로로-3,5-비스 (트피플루오르메틸) 페닐 벤조일 우레아 유도체 및 이의 제조방법 |
| 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 |
| DE19651686A1 (de) * | 1996-12-12 | 1998-06-18 | Bayer Ag | Neue substituierte Phenylketoenole |
| US6391912B1 (en) * | 1996-12-12 | 2002-05-21 | Bayer Aktiengesellschaft | Substituted phenylketoenols |
| DE19705329A1 (de) * | 1997-02-12 | 1998-08-13 | Basf Ag | Dicarbonsäurekristallisate |
| DE19742492A1 (de) | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
| DE19749720A1 (de) | 1997-11-11 | 1999-05-12 | Bayer Ag | Neue substituierte 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 |
-
2000
- 2000-09-05 DE DE10043610A patent/DE10043610A1/de not_active Withdrawn
-
2001
- 2001-08-22 AR ARP010104008A patent/AR032472A1/es active IP Right Grant
- 2001-08-23 BR BRPI0114043-4A patent/BR0114043B1/pt not_active IP Right Cessation
- 2001-08-23 KR KR1020037002160A patent/KR100745448B1/ko not_active Expired - Lifetime
- 2001-08-23 CN CNA2006101059116A patent/CN1915023A/zh active Pending
- 2001-08-23 ES ES01960702T patent/ES2248378T3/es not_active Expired - Lifetime
- 2001-08-23 RU RU2003109757/04A patent/RU2287932C2/ru not_active IP Right Cessation
- 2001-08-23 AT AT01960702T patent/ATE308884T1/de not_active IP Right Cessation
- 2001-08-23 AU AU8211901A patent/AU8211901A/xx active Pending
- 2001-08-23 CN CN01815123A patent/CN1452457A/zh active Pending
- 2001-08-23 AU AU2001282119A patent/AU2001282119B2/en not_active Expired
- 2001-08-23 CA CA002420874A patent/CA2420874C/en not_active Expired - Fee Related
- 2001-08-23 JP JP2002524316A patent/JP2004508308A/ja active Pending
- 2001-08-23 WO PCT/EP2001/009731 patent/WO2002019824A1/de not_active Ceased
- 2001-08-23 EP EP01960702A patent/EP1330161B1/de not_active Expired - Lifetime
- 2001-08-23 DE DE50108034T patent/DE50108034D1/de not_active Expired - Lifetime
- 2001-08-23 IL IL15456401A patent/IL154564A0/xx active IP Right Grant
- 2001-08-23 MX MXPA03001824A patent/MXPA03001824A/es active IP Right Grant
- 2001-08-23 US US10/363,153 patent/US7084138B2/en not_active Expired - Lifetime
- 2001-09-03 TW TW090121713A patent/TWI278282B/zh not_active IP Right Cessation
-
2003
- 2003-02-20 IL IL154564A patent/IL154564A/en not_active IP Right Cessation
- 2003-03-04 ZA ZA200301774A patent/ZA200301774B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1330161A1 (de) | 2003-07-30 |
| JP2004508308A (ja) | 2004-03-18 |
| DE50108034D1 (de) | 2005-12-15 |
| CA2420874C (en) | 2009-04-28 |
| ATE308884T1 (de) | 2005-11-15 |
| TWI278282B (en) | 2007-04-11 |
| IL154564A0 (en) | 2003-09-17 |
| AU2001282119B2 (en) | 2006-08-10 |
| BR0114043B1 (pt) | 2013-05-07 |
| DE10043610A1 (de) | 2002-03-14 |
| AU8211901A (en) | 2002-03-22 |
| KR20030029137A (ko) | 2003-04-11 |
| EP1330161B1 (de) | 2005-11-09 |
| RU2287932C2 (ru) | 2006-11-27 |
| KR100745448B1 (ko) | 2007-08-03 |
| CA2420874A1 (en) | 2003-02-28 |
| ZA200301774B (en) | 2004-03-04 |
| US7084138B2 (en) | 2006-08-01 |
| WO2002019824A1 (de) | 2002-03-14 |
| AR032472A1 (es) | 2003-11-12 |
| US20040038827A1 (en) | 2004-02-26 |
| ES2248378T3 (es) | 2006-03-16 |
| IL154564A (en) | 2009-02-11 |
| MXPA03001824A (es) | 2003-06-04 |
| BR0114043A (pt) | 2003-07-29 |
| CN1452457A (zh) | 2003-10-29 |
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