EA200600134A1 - Гербицидные комбинации с особыми сульфонамидами - Google Patents
Гербицидные комбинации с особыми сульфонамидамиInfo
- Publication number
- EA200600134A1 EA200600134A1 EA200600134A EA200600134A EA200600134A1 EA 200600134 A1 EA200600134 A1 EA 200600134A1 EA 200600134 A EA200600134 A EA 200600134A EA 200600134 A EA200600134 A EA 200600134A EA 200600134 A1 EA200600134 A1 EA 200600134A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- herbicides
- compounds
- group
- flufenacet
- salts
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 4
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 150000003456 sulfonamides Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000005531 Flufenacet Substances 0.000 abstract 2
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 abstract 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 1
- KFEFNHNXZQYTEW-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-4-methylbenzoic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=CC(C)=CC=C1C(O)=O KFEFNHNXZQYTEW-UHFFFAOYSA-N 0.000 abstract 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 abstract 1
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 abstract 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 abstract 1
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 abstract 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 abstract 1
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 abstract 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 abstract 1
- NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 abstract 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 abstract 1
- 239000002890 Aclonifen Substances 0.000 abstract 1
- 239000005484 Bifenox Substances 0.000 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- 239000005494 Chlorotoluron Substances 0.000 abstract 1
- 239000005496 Chlorsulfuron Substances 0.000 abstract 1
- 239000005498 Clodinafop Substances 0.000 abstract 1
- 239000005500 Clopyralid Substances 0.000 abstract 1
- 239000005501 Cycloxydim Substances 0.000 abstract 1
- 239000005504 Dicamba Substances 0.000 abstract 1
- 239000005506 Diclofop Substances 0.000 abstract 1
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005507 Diflufenican Substances 0.000 abstract 1
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 abstract 1
- RXCPQSJAVKGONC-UHFFFAOYSA-N Flumetsulam Chemical compound N1=C2N=C(C)C=CN2N=C1S(=O)(=O)NC1=C(F)C=CC=C1F RXCPQSJAVKGONC-UHFFFAOYSA-N 0.000 abstract 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract 1
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005558 Fluroxypyr Substances 0.000 abstract 1
- 239000005559 Flurtamone Substances 0.000 abstract 1
- 239000005561 Glufosinate Substances 0.000 abstract 1
- 239000005562 Glyphosate Substances 0.000 abstract 1
- LXKOADMMGWXPJQ-UHFFFAOYSA-N Halosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C(O)=O)C)=N1 LXKOADMMGWXPJQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005566 Imazamox Substances 0.000 abstract 1
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005574 MCPA Substances 0.000 abstract 1
- 239000005578 Mesotrione Substances 0.000 abstract 1
- 239000005582 Metosulam Substances 0.000 abstract 1
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005591 Pendimethalin Substances 0.000 abstract 1
- 239000005596 Picolinafen Substances 0.000 abstract 1
- 239000005603 Prosulfocarb Substances 0.000 abstract 1
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 abstract 1
- 239000005618 Sulcotrione Substances 0.000 abstract 1
- 239000005624 Tralkoxydim Substances 0.000 abstract 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005626 Tribenuron Substances 0.000 abstract 1
- 239000005629 Tritosulfuron Substances 0.000 abstract 1
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 abstract 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 abstract 1
- GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 abstract 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 abstract 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 abstract 1
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 abstract 1
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 abstract 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 abstract 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract 1
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 abstract 1
- GINFBXXYGUODAT-UHFFFAOYSA-N flucarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F GINFBXXYGUODAT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 abstract 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 abstract 1
- 229940097068 glyphosate Drugs 0.000 abstract 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 abstract 1
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 abstract 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 abstract 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 abstract 1
- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 abstract 1
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 abstract 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 abstract 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 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 abstract 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 abstract 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 abstract 1
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
- 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
-
- 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<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a 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)
Abstract
Изобретение относится к гербицидной комбинации с эффективным содержанием компонентов (А), (В) и (С) и улучшенными свойствами по защите растений, причем,(А) означает один или несколько гербицидов из группы соединений формулы (I) и их солей(В) означает один или несколько гербицидов из группы соединений формулы (II) и их солей(С) означает один или несколько гербицидов, действующих селективно в некоторых однодольных культурах против однодольных и/или двудольных сорных растений и выбираемых из группы соединений,:(С1) дифлуфеникан, (С2) имазамокс, (С3) флорасулам, (С4) галосульфурон, (С5) тритосульфурон, (С6) пиколинафен, (С7) цинидон-этил, (С8) мезотрионе, (С9) метосулам, (С10) клопиралид, (С11) флуфенацет, (С12) флуметсулам, (С13) флупоксам, (С14) просульфокарб, (С15) флуртамоне, (С16) аклонифен, (С17) феноксапроп, (С18) изопротурон, (С19) диклофоп, (С20) клодинафоп, (С21) хлортолурон, (С22) метабензтиазурон, (С23) имазаметабенз, (С24) тралкоксидим, (С25) дифензокват, (С26) флампроп, (С27) пендиметалин, (С28) мекопроп, (С29) МСРА, (С30) дихлорпроп, (С31) 2,4-D, (C32) дикамба, (С33) флуроксипир, (С34) иоксинил, (С35) бромоксинил, (С36) бифенокс, (С37) флуорогликофен, (С38) лактофен, (С39) пирафлуфен, (С40) флукарбазоне, (С41) бентазон, (С42) флуфенацет, (С43) метсульфурон, (С44) трибенурон, (С45) тифенсульфурон, (С46) триасульфурон, (С47) хлорсульфурон, (С48) флупирсульфурон, (С49) флуазолате, (С50) сульфосульфурон, (С51) глуфосинате, (С52) глифосате, (С53) сулкотрионе, (С54) циклоксидим, (С55) сетоксидим, (С56) клетодим, (С57) карфентразон, (С58) имазетапир, (С59) имазаквин, (С60) имазапир, (С61) имазапик, (С62) бефлубутамид, (С63) фентразамид и (С64) амикарбазоне.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10334304A DE10334304A1 (de) | 2003-07-28 | 2003-07-28 | Herbizid-Kombinationen mit speziellen Sulfonamiden |
| PCT/EP2004/007834 WO2005009133A1 (de) | 2003-07-28 | 2004-07-15 | Herbizid-kombinationen mit speziellen sulfonamiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EA200600134A1 true EA200600134A1 (ru) | 2006-08-25 |
Family
ID=34088886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200600134A EA200600134A1 (ru) | 2003-07-28 | 2004-07-15 | Гербицидные комбинации с особыми сульфонамидами |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20050070437A1 (ru) |
| EP (1) | EP1651047B1 (ru) |
| AR (1) | AR045115A1 (ru) |
| AT (1) | ATE381264T1 (ru) |
| AU (1) | AU2004259166B2 (ru) |
| BR (1) | BRPI0413103A (ru) |
| DE (2) | DE10334304A1 (ru) |
| DK (1) | DK1651047T3 (ru) |
| EA (1) | EA200600134A1 (ru) |
| PL (1) | PL1651047T3 (ru) |
| WO (1) | WO2005009133A1 (ru) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005059470A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| WO2009089165A2 (en) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinations of herbicides and safeners |
| AU2009212525B2 (en) * | 2008-02-05 | 2012-06-21 | Arysta Lifescience North America, Llc | Solid formulation of low melting active compound |
| MX2010008873A (es) * | 2008-02-12 | 2010-08-31 | Arysta Lifescience North Ameri | Metodo para el control de vegetacion indeseada. |
| TW201113377A (en) * | 2009-09-01 | 2011-04-16 | Basf Agrochemical Products Bv | Herbicide-tolerant plants |
| CN102027959B (zh) * | 2009-09-28 | 2013-06-12 | 南京华洲药业有限公司 | 一种含二氯吡啶酸与绿麦隆的增效除草组合物及其应用 |
| UA118765C2 (uk) | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
| PT108561B (pt) * | 2015-06-16 | 2017-07-20 | Sapec Agro S A | Mistura herbicida |
| CN111787799A (zh) * | 2018-02-28 | 2020-10-16 | 拜耳公司 | 减少作物损害的方法 |
| MX2021009954A (es) | 2019-02-19 | 2021-12-10 | Gowan Company L L C | Composiciones liquidas estables y metodos para usar las mismas. |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5534486A (en) * | 1991-04-04 | 1996-07-09 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyl triazolinones having substituents bonded via oxygen |
| DE19520839A1 (de) * | 1995-06-08 | 1996-12-12 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit 4-Iodo-2-[3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) ureidosulfonyl] -benzoesäureestern |
| DE19638887A1 (de) * | 1996-09-23 | 1998-03-26 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
| DE10031825A1 (de) * | 2000-06-30 | 2002-01-10 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
| DE10135642A1 (de) * | 2001-07-21 | 2003-02-27 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| WO2003028450A2 (en) * | 2001-09-27 | 2003-04-10 | Syngenta Participations Ag | Herbicidal composition |
| WO2003028467A1 (en) * | 2001-09-27 | 2003-04-10 | Syngenta Participations Ag | Herbicidal composition |
-
2003
- 2003-07-28 DE DE10334304A patent/DE10334304A1/de not_active Withdrawn
-
2004
- 2004-07-15 WO PCT/EP2004/007834 patent/WO2005009133A1/de not_active Ceased
- 2004-07-15 AU AU2004259166A patent/AU2004259166B2/en not_active Ceased
- 2004-07-15 DK DK04763233T patent/DK1651047T3/da active
- 2004-07-15 PL PL04763233T patent/PL1651047T3/pl unknown
- 2004-07-15 EA EA200600134A patent/EA200600134A1/ru unknown
- 2004-07-15 AT AT04763233T patent/ATE381264T1/de active
- 2004-07-15 EP EP04763233A patent/EP1651047B1/de not_active Expired - Lifetime
- 2004-07-15 DE DE502004005767T patent/DE502004005767D1/de not_active Expired - Lifetime
- 2004-07-15 BR BRPI0413103-7A patent/BRPI0413103A/pt not_active IP Right Cessation
- 2004-07-26 AR ARP040102647A patent/AR045115A1/es active IP Right Grant
- 2004-07-28 US US10/900,849 patent/US20050070437A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AR045115A1 (es) | 2005-10-19 |
| AU2004259166B2 (en) | 2010-06-10 |
| DK1651047T3 (da) | 2008-05-05 |
| WO2005009133A1 (de) | 2005-02-03 |
| BRPI0413103A (pt) | 2006-10-03 |
| US20050070437A1 (en) | 2005-03-31 |
| ATE381264T1 (de) | 2008-01-15 |
| AU2004259166A1 (en) | 2005-02-03 |
| DE10334304A1 (de) | 2005-03-10 |
| DE502004005767D1 (de) | 2008-01-31 |
| EP1651047B1 (de) | 2007-12-19 |
| EP1651047A1 (de) | 2006-05-03 |
| PL1651047T3 (pl) | 2008-05-30 |
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