JP2003523977A5 - - Google Patents
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- JP2003523977A5 JP2003523977A5 JP2001559265A JP2001559265A JP2003523977A5 JP 2003523977 A5 JP2003523977 A5 JP 2003523977A5 JP 2001559265 A JP2001559265 A JP 2001559265A JP 2001559265 A JP2001559265 A JP 2001559265A JP 2003523977 A5 JP2003523977 A5 JP 2003523977A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- substituted
- halogen
- optionally
- Prior art date
- Legal status (The legal status 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 status listed.)
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- 229910052736 halogen Inorganic materials 0.000 description 17
- 150000002367 halogens Chemical class 0.000 description 16
- -1 C 1 -C 6 -alkyl Chemical class 0.000 description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
- 125000006413 ring segment Chemical group 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 description 1
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
- ZCXUVYAZINUVJD-AHXZWLDOSA-N 2-deoxy-2-((18)F)fluoro-alpha-D-glucose Chemical compound OC[C@H]1O[C@H](O)[C@H]([18F])[C@@H](O)[C@@H]1O ZCXUVYAZINUVJD-AHXZWLDOSA-N 0.000 description 1
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 1
- 239000005874 Bifenthrin Substances 0.000 description 1
- 0 C*(C)C(OC(C1(CCCC1)OC1=O)=C1c1c(C)cc(C)cc1*)=O Chemical compound C*(C)C(OC(C1(CCCC1)OC1=O)=C1c1c(C)cc(C)cc1*)=O 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- 239000005895 Esfenvalerate Substances 0.000 description 1
- 239000005896 Etofenprox Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 description 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 description 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
- 229960005424 cypermethrin Drugs 0.000 description 1
- 229960002483 decamethrin Drugs 0.000 description 1
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 1
- NYPJDWWKZLNGGM-RPWUZVMVSA-N esfenvalerate Chemical compound C=1C([C@@H](C#N)OC(=O)[C@@H](C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-RPWUZVMVSA-N 0.000 description 1
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 1
- 229950005085 etofenprox Drugs 0.000 description 1
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000005910 lambda-Cyhalothrin Substances 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 229940108410 resmethrin Drugs 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
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10007411.1 | 2000-02-18 | ||
| DE10007411A DE10007411A1 (de) | 2000-02-18 | 2000-02-18 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| PCT/EP2001/001237 WO2001060158A1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003523977A JP2003523977A (ja) | 2003-08-12 |
| JP2003523977A5 true JP2003523977A5 (enExample) | 2008-04-03 |
| JP4928700B2 JP4928700B2 (ja) | 2012-05-09 |
Family
ID=7631416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001559265A Expired - Lifetime JP4928700B2 (ja) | 2000-02-18 | 2001-02-06 | 殺虫性及び殺ダニ性を含む活性物質の組合わせ |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US6653343B2 (enExample) |
| EP (1) | EP1263287B1 (enExample) |
| 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 |
| AU2007101012B4 (en) * | 2002-12-05 | 2007-11-15 | Osmose (Australia) Pty Limited | Envelope 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 |
| EP2345329B1 (en) | 2003-04-09 | 2019-09-18 | Koppers Performance Chemicals Inc. | Micronized wood preservative formulations |
| 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 |
| US20100112060A1 (en) * | 2006-11-21 | 2010-05-06 | Pesah Maor | 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 |
| US8747875B2 (en) * | 2008-09-29 | 2014-06-10 | The Hartz Mountain Corporation | Photo-stable pest control |
| ES2704028T3 (es) | 2009-04-30 | 2019-03-13 | Water Gremlin Co | Piezas de batería que tienen elementos de retención y sellado y métodos asociados de fabricación y uso |
| US20110129574A1 (en) * | 2009-11-30 | 2011-06-02 | Pathak Chandrashekhar P | Methods and compositions for filling fleshy fruits and vegetables |
| EA022553B1 (ru) | 2010-01-22 | 2016-01-29 | Байер Интеллектуэль Проперти Гмбх | Применение комбинации биологически активных веществ, набор и средство, содержащие комбинацию биологически активных веществ, для борьбы с вредителями животного происхождения и способ улучшения использования продукционного потенциала трансгенного растения |
| BR112012029647A2 (pt) | 2010-05-21 | 2016-08-02 | Chemilia Ab | novos derivados de pirimidinas |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| JP5886411B2 (ja) | 2011-03-24 | 2016-03-16 | ノビガ・リサーチ・エービーＮｏｖｉｇａ Ｒｅｓｅａｒｃｈ ＡＢ | 新規のピリミジン誘導体 |
| 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 |
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-
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 KR KR1020027009781A patent/KR100740977B1/ko not_active Expired - Lifetime
- 2001-02-06 ES ES01902414T patent/ES2244581T3/es not_active Expired - Lifetime
- 2001-02-06 CA CA2400425A patent/CA2400425C/en not_active Expired - Fee Related
- 2001-02-06 IL IL15106801A patent/IL151068A0/xx active IP Right Grant
- 2001-02-06 AT AT01902414T patent/ATE301931T1/de not_active IP Right Cessation
- 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
- 2001-02-06 HU HU0204343A patent/HUP0204343A3/hu unknown
- 2001-02-06 BR BRPI0108427-5A patent/BR0108427B1/pt not_active IP Right Cessation
- 2001-02-06 CN CNB018049605A patent/CN1262187C/zh not_active Expired - Lifetime
- 2001-02-06 DE DE50107115T patent/DE50107115D1/de not_active Expired - Fee Related
- 2001-02-06 US US10/204,011 patent/US6653343B2/en not_active Expired - Lifetime
- 2001-02-06 MX MXPA02008011A patent/MXPA02008011A/es active IP Right Grant
- 2001-02-06 AU AU30249/01A patent/AU775704B2/en not_active Expired
- 2001-02-06 PL PL01356369A patent/PL356369A1/xx not_active Application Discontinuation
- 2001-02-06 EP EP01902414A patent/EP1263287B1/de not_active Expired - Lifetime
- 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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