EA011892B1 - Комбинация гербицида с защитным веществом - Google Patents
Комбинация гербицида с защитным веществом Download PDFInfo
- Publication number
- EA011892B1 EA011892B1 EA200601704A EA200601704A EA011892B1 EA 011892 B1 EA011892 B1 EA 011892B1 EA 200601704 A EA200601704 A EA 200601704A EA 200601704 A EA200601704 A EA 200601704A EA 011892 B1 EA011892 B1 EA 011892B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- carbon atoms
- alkyl
- plants
- halogen
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 23
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 11
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims abstract description 6
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 claims abstract description 5
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 claims abstract description 4
- XXWNKVBJDWSYBN-UHFFFAOYSA-N diethoxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC=CC=C1 XXWNKVBJDWSYBN-UHFFFAOYSA-N 0.000 claims abstract description 4
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- -1 cyano, thiocyanato Chemical group 0.000 claims description 69
- 239000000126 substance Substances 0.000 claims description 57
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- 230000001681 protective effect Effects 0.000 claims description 43
- 229910052739 hydrogen Inorganic materials 0.000 claims description 41
- 239000001257 hydrogen Substances 0.000 claims description 40
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- 125000000217 alkyl group Chemical group 0.000 claims description 35
- 239000013543 active substance Substances 0.000 claims description 29
- 150000002431 hydrogen Chemical class 0.000 claims description 29
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- 238000002360 preparation method Methods 0.000 claims description 22
- 125000003282 alkyl amino group Chemical group 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 18
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- 125000005843 halogen group Chemical group 0.000 claims description 9
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- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 8
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- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 8
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- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
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- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 claims description 2
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- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 abstract description 3
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 abstract description 3
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 abstract description 3
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- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 abstract description 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 abstract description 2
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- LCZGHQHKPPQZSC-UHFFFAOYSA-N n-methoxy-n-[4-(methylcarbamoylamino)phenyl]sulfonylbenzamide Chemical compound C1=CC(NC(=O)NC)=CC=C1S(=O)(=O)N(OC)C(=O)C1=CC=CC=C1 LCZGHQHKPPQZSC-UHFFFAOYSA-N 0.000 abstract 1
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- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 8
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- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 6
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- LYPWWQLKWQNQKV-UHFFFAOYSA-N methyl 2-[5-ethyl-2-[[4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]phenoxy]methyl]phenoxy]propanoate Chemical compound COC(=O)C(C)OC1=CC(CC)=CC=C1COC1=CC=C(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)C=C1 LYPWWQLKWQNQKV-UHFFFAOYSA-N 0.000 description 1
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- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 1
- DEIKMOQTJBGGAX-DJKKODMXSA-N pyriminobac Chemical compound CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(O)=O DEIKMOQTJBGGAX-DJKKODMXSA-N 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
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- IBBLRJGOOANPTQ-JKVLGAQCSA-N quinapril hydrochloride Chemical compound Cl.C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CC2=CC=CC=C2C1)C(O)=O)CC1=CC=CC=C1 IBBLRJGOOANPTQ-JKVLGAQCSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- JRQGDDUXDKCWRF-UHFFFAOYSA-M sodium;n-(2-methoxycarbonylphenyl)sulfonyl-4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carboximidate Chemical compound [Na+].O=C1N(C)C(OCCC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1C(=O)OC JRQGDDUXDKCWRF-UHFFFAOYSA-M 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
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
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- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- 239000008096 xylene Substances 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004015140 | 2004-03-27 | ||
| DE102004031345 | 2004-06-30 | ||
| PCT/EP2005/002672 WO2005092103A1 (de) | 2004-03-27 | 2005-03-12 | Herbizid-safener-kombination |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200601704A1 EA200601704A1 (ru) | 2007-02-27 |
| EA011892B1 true EA011892B1 (ru) | 2009-06-30 |
Family
ID=34962868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200601704A EA011892B1 (ru) | 2004-03-27 | 2005-03-12 | Комбинация гербицида с защитным веществом |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7563749B2 (https=) |
| EP (1) | EP1732391B1 (https=) |
| JP (1) | JP2007530473A (https=) |
| KR (1) | KR20060131926A (https=) |
| AR (1) | AR050143A1 (https=) |
| AT (1) | ATE442044T1 (https=) |
| AU (1) | AU2005226870B2 (https=) |
| BR (1) | BRPI0509289A (https=) |
| CA (1) | CA2560908A1 (https=) |
| CR (1) | CR8557A (https=) |
| DE (1) | DE502005008105D1 (https=) |
| EA (1) | EA011892B1 (https=) |
| ES (1) | ES2329592T3 (https=) |
| IL (1) | IL178033A0 (https=) |
| PL (1) | PL1732391T3 (https=) |
| PT (1) | PT1732391E (https=) |
| UA (1) | UA84201C2 (https=) |
| WO (1) | WO2005092103A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA011812B1 (ru) * | 2004-03-27 | 2009-06-30 | Байер Кропсайенс Аг | Комбинация гербицидов |
| EP1728430A1 (de) * | 2005-06-04 | 2006-12-06 | Bayer CropScience GmbH | Herbizide Mittel |
| US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
| BR122017006111B8 (pt) | 2006-10-31 | 2022-12-06 | Du Pont | Métodos para controlar ervas daninhas |
| EP2145537A1 (en) * | 2008-07-09 | 2010-01-20 | Bayer CropScience AG | Plant growth regulator |
| AU2010209649B2 (en) * | 2009-02-02 | 2015-01-22 | Basf Se | Herbicidal compositions comprising naptalam |
| EP2255637A1 (en) * | 2009-05-02 | 2010-12-01 | Bayer CropScience AG | Method for weed control in lawn or turf |
| BR112012029397B1 (pt) * | 2010-05-17 | 2018-08-28 | Nufarm Australia Ltd | processo para a preparação de sais de amina sólidos de herbicidas à base de ácido carboxílico aromático substituído |
| CN103237894A (zh) | 2010-08-13 | 2013-08-07 | 先锋国际良种公司 | 包含具有羟基苯丙酮酸双加氧酶(hppd)活性的序列的组合物和方法 |
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- 2005-03-12 UA UAA200611344A patent/UA84201C2/ru unknown
- 2005-03-12 WO PCT/EP2005/002672 patent/WO2005092103A1/de not_active Ceased
- 2005-03-12 EA EA200601704A patent/EA011892B1/ru not_active IP Right Cessation
- 2005-03-12 JP JP2007504300A patent/JP2007530473A/ja active Pending
- 2005-03-12 PT PT05716020T patent/PT1732391E/pt unknown
- 2005-03-12 ES ES05716020T patent/ES2329592T3/es not_active Expired - Lifetime
- 2005-03-12 DE DE502005008105T patent/DE502005008105D1/de not_active Expired - Lifetime
- 2005-03-12 KR KR1020067020021A patent/KR20060131926A/ko not_active Ceased
- 2005-03-12 EP EP05716020A patent/EP1732391B1/de not_active Expired - Lifetime
- 2005-03-12 CA CA002560908A patent/CA2560908A1/en not_active Abandoned
- 2005-03-12 AU AU2005226870A patent/AU2005226870B2/en not_active Ceased
- 2005-03-12 AT AT05716020T patent/ATE442044T1/de active
- 2005-03-12 PL PL05716020T patent/PL1732391T3/pl unknown
- 2005-03-23 AR ARP050101172A patent/AR050143A1/es not_active Application Discontinuation
- 2005-03-25 US US11/090,985 patent/US7563749B2/en not_active Expired - Fee Related
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2006
- 2006-08-11 CR CR8557A patent/CR8557A/es not_active Application Discontinuation
- 2006-09-12 IL IL178033A patent/IL178033A0/en unknown
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| EP1008297A2 (de) * | 1990-12-21 | 2000-06-14 | Aventis CropScience GmbH | Mischungen aus Herbiziden und Antidots |
| DE4323122A1 (de) * | 1993-07-10 | 1995-01-12 | Hoechst Schering Agrevo Gmbh | Mischungen aus Herbiziden und Antidots |
| US5476936A (en) * | 1993-09-27 | 1995-12-19 | Bayer Aktiengesellschaft | N-azinyl-N'-(het)arylsulphonyl-ureas |
Also Published As
| Publication number | Publication date |
|---|---|
| PL1732391T3 (pl) | 2010-02-26 |
| AU2005226870A1 (en) | 2005-10-06 |
| IL178033A0 (en) | 2006-12-31 |
| EP1732391A1 (de) | 2006-12-20 |
| UA84201C2 (en) | 2008-09-25 |
| US7563749B2 (en) | 2009-07-21 |
| CR8557A (es) | 2008-02-28 |
| AU2005226870B2 (en) | 2010-06-10 |
| DE502005008105D1 (de) | 2009-10-22 |
| PT1732391E (pt) | 2009-11-18 |
| KR20060131926A (ko) | 2006-12-20 |
| BRPI0509289A (pt) | 2007-09-18 |
| ES2329592T3 (es) | 2009-11-27 |
| EP1732391B1 (de) | 2009-09-09 |
| EA200601704A1 (ru) | 2007-02-27 |
| US20050233904A1 (en) | 2005-10-20 |
| WO2005092103A1 (de) | 2005-10-06 |
| AR050143A1 (es) | 2006-10-04 |
| CA2560908A1 (en) | 2005-10-06 |
| JP2007530473A (ja) | 2007-11-01 |
| ATE442044T1 (de) | 2009-09-15 |
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