UA73175C2 - Selective herbicidal agent on the basis of heteroaryloxyacetamides - Google Patents

Selective herbicidal agent on the basis of heteroaryloxyacetamides Download PDF

Info

Publication number: UA73175C2
Authority: UA; Ukraine
Prior art keywords: methyl; active substances; ethyl; sodium; flufenacet
Prior art date: 2000-05-22

Application number

UA20021210398A

Other languages

English (en)

Ukrainian (uk)

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.)

2000-05-22

Filing date

2001-09-05

Publication date

2005-06-15

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7643120&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UA73175(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2001-05-09 Priority claimed from PCT/EP2001/005242 external-priority patent/WO2001089301A1/de

2001-09-05 Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag

2005-06-15 Publication of UA73175C2 publication Critical patent/UA73175C2/uk

Links

239000004009 herbicide Substances 0.000 title description 9
239000013543 active substance Substances 0.000 abstract description 57
241000196324 Embryophyta Species 0.000 abstract description 37
-1 heteroaryloxy acetamides Chemical class 0.000 abstract description 20
230000002363 herbicidal effect Effects 0.000 abstract description 10
150000001875 compounds Chemical class 0.000 abstract description 9
230000002195 synergetic effect Effects 0.000 abstract description 6
239000000203 mixture Substances 0.000 description 25
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 18
239000000460 chlorine Chemical group 0.000 description 9
229910052801 chlorine Inorganic materials 0.000 description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
239000011737 fluorine Substances 0.000 description 8
229910052731 fluorine Inorganic materials 0.000 description 8
125000001153 fluoro group Chemical group F* 0.000 description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
239000005531 Flufenacet Substances 0.000 description 5
239000005560 Foramsulfuron Substances 0.000 description 5
239000005577 Mesosulfuron Substances 0.000 description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
229910052794 bromium Inorganic materials 0.000 description 5
239000008187 granular material Substances 0.000 description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 description 5
238000000034 method Methods 0.000 description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 description 4
JUJFQMPKBJPSFZ-UHFFFAOYSA-M Iodosulfuron-methyl-sodium Chemical compound [Na+].COC(=O)C1=CC=C(I)C=C1S(=O)(=O)[N-]C(=O)NC1=NC(C)=NC(OC)=N1 JUJFQMPKBJPSFZ-UHFFFAOYSA-M 0.000 description 4
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 description 4
AIMMSOZBPYFASU-UHFFFAOYSA-N n-(4,6-dimethoxypyrimidin-2-yl)-n'-[3-(2,2,2-trifluoroethoxy)pyridin-1-ium-2-yl]sulfonylcarbamimidate Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)OCC(F)(F)F)=N1 AIMMSOZBPYFASU-UHFFFAOYSA-N 0.000 description 4
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
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 4
125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 3
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 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
239000005469 Azimsulfuron Substances 0.000 description 3
PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 3
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 description 3
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
239000005529 Florasulam Substances 0.000 description 3
QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 description 3
239000005566 Imazamox Substances 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
239000000969 carrier Substances 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 description 3
235000013399 edible fruits Nutrition 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
235000013312 flour Nutrition 0.000 description 3
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 description 3
PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
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 description 3
150000004702 methyl esters Chemical class 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
239000002480 mineral oil Substances 0.000 description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000011435 rock Substances 0.000 description 3
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 3
235000015112 vegetable and seed oil Nutrition 0.000 description 3
239000008158 vegetable oil Substances 0.000 description 3
125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 description 2
MHULQDZDXMHODA-UHFFFAOYSA-N 1-(2,2-dichloroacetyl)-3,3,8a-trimethyl-2,4,7,8-tetrahydropyrrolo[1,2-a]pyrimidin-6-one Chemical compound C1C(C)(C)CN(C(=O)C(Cl)Cl)C2(C)N1C(=O)CC2 MHULQDZDXMHODA-UHFFFAOYSA-N 0.000 description 2
OJMROTIHMXNNBF-UHFFFAOYSA-N 1-(2-chlorophenyl)-5-phenylpyrazole-3-carboxylic acid Chemical compound C=1C=CC=C(Cl)C=1N1N=C(C(=O)O)C=C1C1=CC=CC=C1 OJMROTIHMXNNBF-UHFFFAOYSA-N 0.000 description 2
125000006021 1-methyl-2-propenyl group Chemical group 0.000 description 2
MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 description 2
KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 description 2
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 2
VIQBLZHDBUVBDS-UHFFFAOYSA-N 2-heptan-2-yloxyheptane Chemical compound CCCCCC(C)OC(C)CCCCC VIQBLZHDBUVBDS-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
239000005711 Benzoic acid Substances 0.000 description 2
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SRCPGSKDFKGYHP-UHFFFAOYSA-N methyl 2-(carbamoylsulfamoyl)benzoate Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(N)=O SRCPGSKDFKGYHP-UHFFFAOYSA-N 0.000 description 1
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CHEDHKBPPDKBQF-UPONEAKYSA-N n-[5-[(6s,7ar)-6-fluoro-1,3-dioxo-5,6,7,7a-tetrahydropyrrolo[1,2-c]imidazol-2-yl]-2-chloro-4-fluorophenyl]-1-chloromethanesulfonamide Chemical compound N1([C@@H](C2=O)C[C@@H](C1)F)C(=O)N2C1=CC(NS(=O)(=O)CCl)=C(Cl)C=C1F CHEDHKBPPDKBQF-UPONEAKYSA-N 0.000 description 1
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UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
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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 description 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 description 1
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APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
USSIUIGPBLPCDF-KEBDBYFISA-N pyriminobac-methyl Chemical group CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC USSIUIGPBLPCDF-KEBDBYFISA-N 0.000 description 1
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235000019355 sepiolite Nutrition 0.000 description 1
239000002356 single layer Substances 0.000 description 1
JKPSVOHVUGMYGH-UHFFFAOYSA-M sodium;(4,6-dimethoxypyrimidin-2-yl)-[[3-methoxycarbonyl-6-(trifluoromethyl)pyridin-2-yl]sulfonylcarbamoyl]azanide Chemical compound [Na+].COC(=O)C1=CC=C(C(F)(F)F)N=C1S(=O)(=O)NC(=O)[N-]C1=NC(OC)=CC(OC)=N1 JKPSVOHVUGMYGH-UHFFFAOYSA-M 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
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239000000454 talc Substances 0.000 description 1
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OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
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150000003852 triazoles Chemical class 0.000 description 1
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239000011701 zinc 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms

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)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

UA20021210398A 2000-05-22 2001-09-05 Selective herbicidal agent on the basis of heteroaryloxyacetamides UA73175C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10025306		2000-05-22
PCT/EP2001/005242 WO2001089301A1 (de)	2000-05-22	2001-05-09	Selektive herbizide auf basis von heteroaryloxy-acetamiden

Publications (1)

Publication Number	Publication Date
UA73175C2 true UA73175C2 (en)	2005-06-15

Family

ID=7643120

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA20021210398A UA73175C2 (en)	2000-05-22	2001-09-05	Selective herbicidal agent on the basis of heteroaryloxyacetamides

Country Status (13)

Country	Link
EP (11)	EP2243370A2 (pt)
AR (1)	AR035572A1 (pt)
BG (1)	BG65940B1 (pt)
DE (1)	DE10041619A1 (pt)
DK (5)	DK2243364T3 (pt)
ES (5)	ES2535751T3 (pt)
HU (9)	HU230837B1 (pt)
PL (2)	PL218352B1 (pt)
PT (5)	PT2243364E (pt)
RU (1)	RU2273994C2 (pt)
UA (1)	UA73175C2 (pt)
YU (1)	YU87402A (pt)
ZA (1)	ZA200208479B (pt)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2927071T3 (es)	2014-02-06	2022-11-02	Gambro Lundia Ab	Hemodializador para purificar la sangre
KR102346383B1 (ko)	2014-02-06	2022-01-04	감브로 룬디아 아베	혈액 정화를 위한 멤브레인
GB2532217B (en) *	2014-11-11	2019-05-15	Rotam Agrochem Int Co Ltd	Herbicidal composition and method for controlling plant growth
GB2532218B (en) *	2014-11-11	2019-11-20	Rotam Agrochem Int Co Ltd	Herbicidal composition and method for controlling plant growth
RU2698056C1 (ru) *	2018-12-26	2019-08-21	АО "Щелково Агрохим"	Синергетическая гербицидная композиция
BR102020019866A2 (pt) *	2020-09-28	2022-04-12	Upl Do Brasil Industria E Comercio De Insumos Agropecuarios S.A.	Combinações de herbicidas cloroacetanilida com fitoprotetores
BE1028935B1 (nl)	2020-12-22	2022-07-19	Globachem	Herbicide preparaten

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2961415D1 (en)	1978-05-20	1982-01-28	Bayer Ag	Heteroaryloxy-acetamides, process for their preparation and their use as herbicides
EP0018497B1 (de)	1979-04-06	1982-04-28	Bayer Ag	Azolyloxy-essigsäureamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
DE2946524A1 (de)	1979-11-17	1981-06-11	Bayer Ag, 5090 Leverkusen	Azolyloxy-carbonsaeure-n-oxy-amide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
EP0094514B1 (en)	1982-05-17	1988-08-10	International Business Machines Corporation	Designation of footnotes and footnote references
DE3228131A1 (de)	1982-07-28	1984-02-02	Bayer Ag, 5090 Leverkusen	Substituierte 3-trichlormethyl-1,2,4-thiadiazol-5-yl-oxyessigsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE3228147A1 (de)	1982-07-28	1984-02-09	Bayer Ag, 5090 Leverkusen	Substituierte 3-trihalogenmethyl-1,2,4-thiadiazol-5-yl-oxyessigsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE3418168A1 (de)	1984-05-16	1985-11-21	Bayer Ag, 5090 Leverkusen	6-chlorbenzazolyloxyacetamide
DE3418167A1 (de)	1984-05-16	1985-11-21	Bayer Ag, 5090 Leverkusen	Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen heteroaryloxyacetamiden
DE3505902A1 (de)	1985-02-21	1986-08-21	Bayer Ag, 5090 Leverkusen	4,5-disubstituierte 1,3-thiazol-2-yloxyacetamide
DE3821600A1 (de)	1988-06-27	1989-12-28	Bayer Ag	Heteroaryloxyessigsaeure-n-isopropylanilide
DE3821597A1 (de)	1988-06-27	1989-12-28	Bayer Ag	5-difluormethyl-1,3,4-thiadiazol-2-yl- oxyessigsaeureamide, verfahren und 5-difluormethyl-2- methylsulfonyl- bzw. 2- methylthio-1,3,4-thiadiazol als zwischenprodukte zu ihrer herstellung und ihre verwendung als selektivherbizide
DE4039810C1 (pt)	1990-12-13	1991-10-17	Mtu Muenchen Gmbh
DE4223465A1 (de)	1992-07-16	1994-01-20	Bayer Ag	Herbizide Mittel auf Basis von Heteroaryloxyacetamiden
FR2722371B1 (fr) *	1994-07-12	1996-08-30	Salomon Sa	Ensemble chaussure/ dispositif de retenue de la chaussure sur un organe de glisse
DE4317323A1 (de)	1993-05-25	1994-12-01	Bayer Ag	N-(4-Fluor-phenyl)-heteroaryloxyacetamide
DE4431219A1 (de)	1994-09-02	1996-03-07	Bayer Ag	Selektive Herbizide auf Basis von Aryluracilen
DE4437049A1 (de)	1994-10-17	1996-04-18	Bayer Ag	Selektive Herbizide auf Basis von Carbamoyltriazolinonen und Heteroaryloxyacetamiden
GB9424853D0 (en)	1994-12-09	1995-02-08	Bayer Ag	New herbicidal compositions
DE19546751B4 (de) *	1994-12-23	2005-02-17	Bayer Cropscience Ag	Selektive Herbizide auf Basis von Heteroaryloxy-acetamiden
ES2128984B1 (es)	1996-05-24	2000-02-01	Bayer Ag	Herbicidas a base de heteroariloxi-acetamidas para el empleo en el cultivo de arroz.
DE19728568B4 (de) *	1996-07-17	2007-06-14	Bayer Cropscience Ag	Herbizide Mittel auf Basis von (5-Trifluormethyl-1,3,4-thiadiazol-2-yl-oxy)-essigsäure-N-isopropyl-N-(4fluorphenyl)-amid
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DE19634701A1 (de)	1996-08-28	1998-03-05	Bayer Ag	Herbizide Mittel auf Basis von 4-Brom-l-methyl-5-trifluormethyl-3-(2-fluor-4-chlor-5-isopropoxycarbonsylphenyl)pyrazol
AR012651A1 (es) *	1997-05-06	2000-11-08	Sumitomo Chemical Co	COMPOSICIoN HERBICIDA Y METODO DE DESMALEZADO UTILIZANDO LA MISMA.
JP4200559B2 (ja) *	1998-10-23	2008-12-24	住友化学株式会社	除草剤組成物

2000
- 2000-08-24 DE DE10041619A patent/DE10041619A1/de not_active Withdrawn
2001
- 2001-04-27 AR ARP010102005A patent/AR035572A1/es active IP Right Grant
- 2001-05-09 PL PL390259A patent/PL218352B1/pl unknown
- 2001-05-09 EP EP10158933A patent/EP2243370A2/de not_active Withdrawn
- 2001-05-09 DK DK10158917T patent/DK2243364T3/en active
- 2001-05-09 EP EP10158924A patent/EP2243366A3/de not_active Withdrawn
- 2001-05-09 ES ES10158917.4T patent/ES2535751T3/es not_active Expired - Lifetime
- 2001-05-09 EP EP10158918A patent/EP2243365A3/de not_active Withdrawn
- 2001-05-09 ES ES05005219.0T patent/ES2535708T3/es not_active Expired - Lifetime
- 2001-05-09 PT PT101589174T patent/PT2243364E/pt unknown
- 2001-05-09 PT PT101589158T patent/PT2243362E/pt unknown
- 2001-05-09 ES ES10158913T patent/ES2531261T3/es not_active Expired - Lifetime
- 2001-05-09 EP EP10158917.4A patent/EP2243364B1/de not_active Expired - Lifetime
- 2001-05-09 HU HU1500631A patent/HU230837B1/hu unknown
- 2001-05-09 RU RU2002134758/04A patent/RU2273994C2/ru active
- 2001-05-09 HU HU1500634A patent/HU230521B1/hu unknown
- 2001-05-09 EP EP05005219.0A patent/EP1552746B1/de not_active Expired - Lifetime
- 2001-05-09 PT PT10158913T patent/PT2243361E/pt unknown
- 2001-05-09 EP EP10158915.8A patent/EP2243362B1/de not_active Revoked
- 2001-05-09 YU YU87402A patent/YU87402A/sh unknown
- 2001-05-09 HU HU1500630A patent/HU230836B1/hu unknown
- 2001-05-09 HU HU1500637A patent/HU230840B1/hu unknown
- 2001-05-09 HU HU1500629A patent/HU230520B1/hu unknown
- 2001-05-09 ES ES10158915.8T patent/ES2533496T3/es not_active Expired - Lifetime
- 2001-05-09 HU HU1500632A patent/HU230838B1/hu unknown
- 2001-05-09 EP EP10158916.6A patent/EP2243363B1/de not_active Expired - Lifetime
- 2001-05-09 EP EP10158932A patent/EP2243369A3/de not_active Withdrawn
- 2001-05-09 PT PT10158916T patent/PT2243363E/pt unknown
- 2001-05-09 EP EP10158929A patent/EP2243368A3/de not_active Withdrawn
- 2001-05-09 HU HU1500635A patent/HU230475B1/hu unknown
- 2001-05-09 HU HU1500636A patent/HU230839B1/hu unknown
- 2001-05-09 DK DK10158915T patent/DK2243362T3/en active
- 2001-05-09 ES ES10158916T patent/ES2531196T3/es not_active Expired - Lifetime
- 2001-05-09 DK DK10158913T patent/DK2243361T3/en active
- 2001-05-09 EP EP10158913.3A patent/EP2243361B1/de not_active Expired - Lifetime
- 2001-05-09 EP EP10158925A patent/EP2243367A3/de not_active Withdrawn
- 2001-05-09 PT PT50052190T patent/PT1552746E/pt unknown
- 2001-05-09 DK DK10158916T patent/DK2243363T3/en active
- 2001-05-09 DK DK05005219.0T patent/DK1552746T3/en active
- 2001-05-09 PL PL394461A patent/PL394461A1/pl not_active Application Discontinuation
- 2001-05-09 HU HU1500628A patent/HU230835B1/hu unknown
- 2001-09-05 UA UA20021210398A patent/UA73175C2/uk unknown
2002
- 2002-10-21 ZA ZA200208479A patent/ZA200208479B/en unknown
- 2002-11-14 BG BG107274A patent/BG65940B1/bg unknown

Also Published As

Publication number	Publication date
HUP1500634A2 (en)	2003-09-29
BG65940B1 (bg)	2010-06-30
EP1552746A1 (de)	2005-07-13
EP2243364A3 (de)	2012-08-08
ZA200208479B (en)	2004-03-09
EP2243362A3 (de)	2012-08-08
ES2533496T3 (es)	2015-04-10
HU230475B1 (hu)	2016-07-28
EP2243363B1 (de)	2014-11-26
EP2243361A2 (de)	2010-10-27
EP1552746B1 (de)	2015-02-11
DK2243361T3 (en)	2015-03-02
DK2243362T3 (en)	2015-03-30
EP2243365A2 (de)	2010-10-27
EP2243366A3 (de)	2012-08-08
HUP1500636A2 (en)	2003-09-29
EP2243362B1 (de)	2014-12-24
PT2243363E (pt)	2015-03-02
EP2243367A3 (de)	2012-08-08
EP2243366A2 (de)	2010-10-27
ES2531196T3 (es)	2015-03-11
AR035572A1 (es)	2004-06-16
BG107274A (bg)	2003-07-31
HU230836B1 (en)	2018-08-28
HUP1500637A2 (en)	2003-09-29
DK1552746T3 (en)	2015-05-04
HU230521B1 (hu)	2016-10-28
HU230840B1 (en)	2018-08-28
EP2243369A3 (de)	2012-08-08
DK2243364T3 (en)	2015-05-04
DE10041619A1 (de)	2001-11-29
EP2243364B1 (de)	2015-04-08
PL394461A1 (pl)	2011-08-16
HUP1500629A2 (en)	2003-08-29
EP2243361A3 (de)	2012-08-08
EP2243363A3 (de)	2012-08-08
RU2273994C2 (ru)	2006-04-20
PT2243362E (pt)	2015-04-08
PT2243364E (pt)	2015-05-27
EP2243369A2 (de)	2010-10-27
PT1552746E (pt)	2015-05-25
EP2243365A3 (de)	2012-08-15
DK2243363T3 (en)	2015-03-02
EP2243364A2 (de)	2010-10-27
HU230838B1 (en)	2018-08-28
EP2243367A2 (de)	2010-10-27
EP2243368A2 (de)	2010-10-27
HUP1500630A3 (en)	2008-08-28
HU230839B1 (en)	2018-08-28
HU230837B1 (en)	2018-08-28
HUP1500635A2 (pt)	2003-09-29
PL218352B1 (pl)	2014-11-28
HUP1500632A2 (en)	2003-09-29
EP2243368A3 (de)	2012-08-08
YU87402A (sh)	2006-01-16
HUP1500631A2 (en)	2003-09-29
ES2531261T3 (es)	2015-03-12
EP2243361B1 (de)	2014-11-26
ES2535751T3 (es)	2015-05-14
ES2535708T3 (es)	2015-05-14
EP2243363A2 (de)	2010-10-27
HUP1500628A2 (en)	2003-09-29
HUP1500630A2 (en)	2003-05-15
EP2243370A2 (de)	2010-10-27
EP2243362A2 (de)	2010-10-27
HU230520B1 (hu)	2016-10-28
HU230835B1 (en)	2018-08-28
PT2243361E (pt)	2015-03-02

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