TN2010000181A1 - Herbicidal combination - Google Patents

Herbicidal combination

Info

Publication number: TN2010000181A1
Authority: TN; Tunisia
Prior art keywords: alkyl; ion; substituted; optionally; group
Prior art date: 2007-10-24

Application number

TN2010000181A

Other languages

English (en)

Inventor

Erwin Hacker

Christian Waldraff

Dominique 3Schreiber

Martin Jeffrey Hills

Dieter Feucht

Klaus-Helmut Muller

Ernst Rudolf Gesing

Georg Bonfig-Picard

Original Assignee

Bayer Cropscience Ag

Priority date (The priority date 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 date listed.)

2007-10-24

Filing date

2010-04-23

Publication date

2011-11-11

2010-04-23 Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag

2011-11-11 Publication of TN2010000181A1 publication Critical patent/TN2010000181A1/fr

Links

230000002363 herbicidal effect Effects 0.000 title abstract 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
150000002500 ions Chemical class 0.000 abstract 3
-1 phosphonium ion Chemical class 0.000 abstract 3
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
LUZZPGJQJKMMDM-JTQLQIEISA-N [(2s)-1-ethoxy-1-oxopropan-2-yl] 2-chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoate Chemical group C1=C(Cl)C(C(=O)O[C@@H](C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 LUZZPGJQJKMMDM-JTQLQIEISA-N 0.000 abstract 2
239000004009 herbicide Substances 0.000 abstract 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
IPPAUTOBDWNELX-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group C1=C([N+]([O-])=O)C(C(=O)OCC(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 IPPAUTOBDWNELX-UHFFFAOYSA-N 0.000 abstract 1
SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 abstract 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 abstract 1
BACHBFVBHLGWSL-SNVBAGLBSA-N (R)-diclofop-methyl Chemical group C1=CC(O[C@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-SNVBAGLBSA-N 0.000 abstract 1
WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 abstract 1
ADDQHLREJDZPMT-AWEZNQCLSA-N (S)-metamifop Chemical compound O=C([C@@H](OC=1C=CC(OC=2OC3=CC(Cl)=CC=C3N=2)=CC=1)C)N(C)C1=CC=CC=C1F ADDQHLREJDZPMT-AWEZNQCLSA-N 0.000 abstract 1
VQHHIQJPQOLZGF-UHFFFAOYSA-N 1-(2-iodophenyl)sulfonyl-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)I)=N1 VQHHIQJPQOLZGF-UHFFFAOYSA-N 0.000 abstract 1
KNGWEAQJZJKFLI-UHFFFAOYSA-N 2,2-dimethyl-4h-1,3-benzodioxine-6-carbaldehyde Chemical compound O=CC1=CC=C2OC(C)(C)OCC2=C1 KNGWEAQJZJKFLI-UHFFFAOYSA-N 0.000 abstract 1
239000002794 2,4-DB Substances 0.000 abstract 1
YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 abstract 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 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
YNTJKQDWYXUTLZ-UHFFFAOYSA-N 2-(3-chlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=CC(Cl)=C1 YNTJKQDWYXUTLZ-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
GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 abstract 1
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 1
ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 abstract 1
239000002890 Aclonifen Substances 0.000 abstract 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
239000005484 Bifenox Substances 0.000 abstract 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
239000005502 Cyhalofop-butyl Substances 0.000 abstract 1
TYIYMOAHACZAMQ-CQSZACIVSA-N Cyhalofop-butyl Chemical group C1=CC(O[C@H](C)C(=O)OCCCC)=CC=C1OC1=CC=C(C#N)C=C1F TYIYMOAHACZAMQ-CQSZACIVSA-N 0.000 abstract 1
239000005505 Dichlorprop-P Substances 0.000 abstract 1
239000005565 Haloxyfop-P Substances 0.000 abstract 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 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
AZFKQCNGMSSWDS-UHFFFAOYSA-N MCPA-thioethyl Chemical group CCSC(=O)COC1=CC=C(Cl)C=C1C AZFKQCNGMSSWDS-UHFFFAOYSA-N 0.000 abstract 1
239000005575 MCPB Substances 0.000 abstract 1
101150039283 MCPB gene Proteins 0.000 abstract 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
239000005576 Mecoprop-P Substances 0.000 abstract 1
239000005590 Oxyfluorfen Substances 0.000 abstract 1
OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 abstract 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
239000005600 Propaquizafop Substances 0.000 abstract 1
239000005609 Quizalofop-P 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
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 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
229910052783 alkali metal Inorganic materials 0.000 abstract 1
150000001340 alkali metals Chemical class 0.000 abstract 1
229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
150000001342 alkaline earth metals Chemical class 0.000 abstract 1
125000003118 aryl group Chemical group 0.000 abstract 1
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
229910052794 bromium Inorganic materials 0.000 abstract 1
VAIZTNZGPYBOGF-UHFFFAOYSA-N butyl 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OCCCC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 VAIZTNZGPYBOGF-UHFFFAOYSA-N 0.000 abstract 1
229910052791 calcium Inorganic materials 0.000 abstract 1
239000011575 calcium Substances 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
150000001768 cations Chemical class 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
JBDHZKLJNAIJNC-LLVKDONJSA-N clodinafop-propargyl Chemical group C1=CC(O[C@H](C)C(=O)OCC#C)=CC=C1OC1=NC=C(Cl)C=C1F JBDHZKLJNAIJNC-LLVKDONJSA-N 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
229910052802 copper Inorganic materials 0.000 abstract 1
239000010949 copper Substances 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
125000004122 cyclic group Chemical group 0.000 abstract 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 1
PQKBPHSEKWERTG-LLVKDONJSA-N ethyl (2r)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoate Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-LLVKDONJSA-N 0.000 abstract 1
VAIZTNZGPYBOGF-CYBMUJFWSA-N fluazifop-P-butyl Chemical group C1=CC(O[C@H](C)C(=O)OCCCC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 VAIZTNZGPYBOGF-CYBMUJFWSA-N 0.000 abstract 1
229910052731 fluorine Inorganic materials 0.000 abstract 1
BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
GOCUAJYOYBLQRH-MRVPVSSYSA-N haloxyfop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-MRVPVSSYSA-N 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
229910052740 iodine Inorganic materials 0.000 abstract 1
229910052742 iron Inorganic materials 0.000 abstract 1
CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-UHFFFAOYSA-N 0.000 abstract 1
229910052744 lithium Inorganic materials 0.000 abstract 1
229910052749 magnesium Inorganic materials 0.000 abstract 1
239000011777 magnesium Substances 0.000 abstract 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 1
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
229910052700 potassium Inorganic materials 0.000 abstract 1
239000011591 potassium Substances 0.000 abstract 1
FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 abstract 1
ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 abstract 1
BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 abstract 1
229920006395 saturated elastomer Polymers 0.000 abstract 1
229910052708 sodium Inorganic materials 0.000 abstract 1
239000011734 sodium Substances 0.000 abstract 1
125000001424 substituent group Chemical group 0.000 abstract 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 abstract 1
229910052723 transition metal Inorganic materials 0.000 abstract 1
150000003624 transition metals Chemical class 0.000 abstract 1
239000011701 zinc Substances 0.000 abstract 1
229910052725 zinc Inorganic materials 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

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)

TN2010000181A 2007-10-24 2010-04-23 Herbicidal combination TN2010000181A1 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP07020850A EP2052607A1 (fr)	2007-10-24	2007-10-24	Combinaison d'herbicide
PCT/EP2008/008952 WO2009053063A2 (fr)	2007-10-24	2008-10-22	Combinaison herbicide

Publications (1)

Publication Number	Publication Date
TN2010000181A1 true TN2010000181A1 (en)	2011-11-11

Family

ID=39432195

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TN2010000181A TN2010000181A1 (en)	2007-10-24	2010-04-23	Herbicidal combination

Country Status (14)

Country	Link
US (1)	US20100311586A1 (fr)
EP (2)	EP2052607A1 (fr)
JP (1)	JP2011500746A (fr)
CN (1)	CN101835378A (fr)
AR (1)	AR068992A1 (fr)
AU (1)	AU2008315613A1 (fr)
BR (1)	BRPI0818880A2 (fr)
CA (1)	CA2703613A1 (fr)
CL (1)	CL2008003149A1 (fr)
EA (1)	EA201000521A1 (fr)
MA (1)	MA31787B1 (fr)
MX (1)	MX2010004533A (fr)
TN (1)	TN2010000181A1 (fr)
WO (1)	WO2009053063A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2011076731A1 (fr) *	2009-12-23	2011-06-30	Bayer Cropscience Ag	Formulation liquide de 2-iodo-n-[(4-méthoxy-6-méthyl-1, 3, 5-triazin-2-yl) carbamoyl] benzène sulfonamide
CN107372566A (zh) *	2017-08-11	2017-11-24	北京科发伟业农药技术中心	一种含噻酮磺隆和iofensulfuron的除草组合物

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CA1215924A (fr)	1983-07-27	1986-12-30	David W. Bewick	Preparation d'acides aryloxypropioniques optiquement actifs et de leurs derives, utiles comme herbicides
BR8404834A (pt)	1983-09-26	1985-08-13	Agrigenetics Res Ass	Metodo para modificar geneticamente uma celula vegetal
JPS6087254A (ja)	1983-10-19	1985-05-16	Japan Carlit Co Ltd:The	新規尿素化合物及びそれを含有する除草剤
BR8600161A (pt)	1985-01-18	1986-09-23	Plant Genetic Systems Nv	Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio
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ATE84302T1 (de)	1988-10-20	1993-01-15	Ciba Geigy Ag	Sulfamoylphenylharnstoffe.
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DE3939010A1 (de)	1989-11-25	1991-05-29	Hoechst Ag	Isoxazoline, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschuetzende mittel
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ATE241007T1 (de)	1990-03-16	2003-06-15	Calgene Llc	Dnas, die für pflanzliche desaturasen kodieren und deren anwendungen
ATE212670T1 (de)	1990-06-18	2002-02-15	Monsanto Technology Llc	Erhöhter stärkegehalt in pflanzen
DE4029304A1 (de)	1990-09-15	1992-03-19	Hoechst Ag	Synergistische herbizide mittel
DE4038430A1 (de)	1990-12-01	1992-06-04	Basf Ag	Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide
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SE467358B (sv)	1990-12-21	1992-07-06	Amylogene Hb	Genteknisk foeraendring av potatis foer bildning av staerkelse av amylopektintyp
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TW259690B (fr)	1992-08-01	1995-10-11	Hoechst Ag
DE4230933A1 (de)	1992-09-16	1994-03-17	Hoechst Ag	Hydroxylamino-phenylsulfonylharnstoffe, Darstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DE4331448A1 (de)	1993-09-16	1995-03-23	Hoechst Schering Agrevo Gmbh	Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener
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DE19534910A1 (de) *	1995-09-20	1997-03-27	Basf Ag	Herbizide Mischungen mit synergistischer Wirkung
DE19621522A1 (de)	1996-05-29	1997-12-04	Hoechst Schering Agrevo Gmbh	Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
WO1998013361A1 (fr)	1996-09-26	1998-04-02	Novartis Ag	Composition herbicide
DE19652961A1 (de)	1996-12-19	1998-06-25	Hoechst Schering Agrevo Gmbh	Neue 2-Fluoracrylsäurederivate, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
US6071856A (en)	1997-03-04	2000-06-06	Zeneca Limited	Herbicidal compositions for acetochlor in rice
DE19727410A1 (de)	1997-06-27	1999-01-07	Hoechst Schering Agrevo Gmbh	3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel
DE19742951A1 (de)	1997-09-29	1999-04-15	Hoechst Schering Agrevo Gmbh	Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung
TW561153B (en)	1998-07-25	2003-11-11	Dongbu Hannong Chemical Co Ltd	Herbicidal phenoxypropionic acid N-alkyl-N-2-fluoro-phenyl amide compounds
AR031027A1 (es)	2000-10-23	2003-09-03	Syngenta Participations Ag	Composiciones agroquimicas
DE10111649A1 (de)	2001-03-12	2002-09-19	Bayer Ag	Substituierte Fluoralkoxyphenylsulfonylharnstoffe
KR20060002857A (ko)	2003-03-26	2006-01-09	바이엘 크롭사이언스 게엠베하	독성 완화제로서의 방향족 하이드록시 화합물의 용도
DE10335725A1 (de)	2003-08-05	2005-03-03	Bayer Cropscience Gmbh	Safener auf Basis aromatisch-aliphatischer Carbonsäuredarivate
DE10335726A1 (de)	2003-08-05	2005-03-03	Bayer Cropscience Gmbh	Verwendung von Hydroxyaromaten als Safener
DE102004023332A1 (de)	2004-05-12	2006-01-19	Bayer Cropscience Gmbh	Chinoxalin-2-on-derivate, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung und deren Verwendung
DE102004035137A1 (de)	2004-07-20	2006-02-16	Bayer Cropscience Gmbh	Wirkstoffe zur Steigerung der Pathogenabwehr in Pflanzen und Methoden zu ihrer Auffindung
EP1717232A1 (fr) *	2005-04-28	2006-11-02	Bayer CropScience GmbH	Urées phénylsulfonyles ayant une activité herbicide
WO2007023719A1 (fr)	2005-08-22	2007-03-01	Kumiai Chemical Industry Co., Ltd.	Agent servant à réduire l'attaque chimique et composition herbicide produisant une attaque chimique réduite
JPWO2007023764A1 (ja)	2005-08-26	2009-02-26	クミアイ化学工業株式会社	薬害軽減剤及び薬害が軽減された除草剤組成物

2007
- 2007-10-24 EP EP07020850A patent/EP2052607A1/fr not_active Withdrawn
2008
- 2008-10-22 US US12/739,107 patent/US20100311586A1/en not_active Abandoned
- 2008-10-22 WO PCT/EP2008/008952 patent/WO2009053063A2/fr not_active Ceased
- 2008-10-22 MX MX2010004533A patent/MX2010004533A/es not_active Application Discontinuation
- 2008-10-22 EA EA201000521A patent/EA201000521A1/ru unknown
- 2008-10-22 CA CA2703613A patent/CA2703613A1/fr not_active Abandoned
- 2008-10-22 JP JP2010530340A patent/JP2011500746A/ja active Pending
- 2008-10-22 AU AU2008315613A patent/AU2008315613A1/en not_active Abandoned
- 2008-10-22 BR BRPI0818880-7A2A patent/BRPI0818880A2/pt not_active Application Discontinuation
- 2008-10-22 EP EP08841658A patent/EP2209378A2/fr not_active Withdrawn
- 2008-10-22 AR ARP080104602A patent/AR068992A1/es unknown
- 2008-10-22 CN CN200880112871A patent/CN101835378A/zh active Pending
- 2008-10-24 CL CL2008003149A patent/CL2008003149A1/es unknown
2010
- 2010-04-23 MA MA32788A patent/MA31787B1/fr unknown
- 2010-04-23 TN TN2010000181A patent/TN2010000181A1/fr unknown

Also Published As

Publication number	Publication date
MA31787B1 (fr)	2010-10-01
AU2008315613A1 (en)	2009-04-30
EP2052607A1 (fr)	2009-04-29
WO2009053063A3 (fr)	2010-03-25
CN101835378A (zh)	2010-09-15
WO2009053063A2 (fr)	2009-04-30
CL2008003149A1 (es)	2009-03-06
MX2010004533A (es)	2010-05-05
BRPI0818880A2 (pt)	2014-10-07
EP2209378A2 (fr)	2010-07-28
AR068992A1 (es)	2009-12-23
JP2011500746A (ja)	2011-01-06
CA2703613A1 (fr)	2009-04-30
EA201000521A1 (ru)	2010-10-29
US20100311586A1 (en)	2010-12-09

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