SK287091B6 - Kombinácia herbicídov, spôsob ničenia škodlivých rastlín a použitie kombinácií herbicídov na ničenie škodlivých rastlín - Google Patents

Kombinácia herbicídov, spôsob ničenia škodlivých rastlín a použitie kombinácií herbicídov na ničenie škodlivých rastlín Download PDF

Info

Publication number: SK287091B6
Authority: SK; Slovakia
Prior art keywords: group; carbon atoms; substituted; alkyl; unsubstituted
Prior art date: 1998-09-18

Application number

SK377-2001A

Other languages

English (en)

Slovak (sk)

Other versions

SK3772001A3 (en

Inventor

Erwin Hacker

Hermann Bieringer

Thomas Auler

Lothar Willms

Klemens Minn

Jens Hollander

J�Rgen Zindel

Wolfgang Giencke

Original Assignee

Bayer Cropscience Aktiengesellschaft

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.)

1998-09-18

Filing date

1999-09-20

Publication date

2009-11-05

1999-09-20 Application filed by Bayer Cropscience Aktiengesellschaft filed Critical Bayer Cropscience Aktiengesellschaft

2001-09-11 Publication of SK3772001A3 publication Critical patent/SK3772001A3/sk

2009-11-05 Publication of SK287091B6 publication Critical patent/SK287091B6/sk

Links

239000004009 herbicide Substances 0.000 title claims abstract description 57
230000002363 herbicidal effect Effects 0.000 title claims abstract description 44
238000000034 method Methods 0.000 title claims abstract description 19
239000013543 active substance Substances 0.000 title claims description 46
239000002689 soil Substances 0.000 claims abstract description 15
QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 claims abstract description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 194
-1 cyano, nitro, thiocyanato Chemical group 0.000 claims description 113
125000000217 alkyl group Chemical group 0.000 claims description 74
150000003254 radicals Chemical class 0.000 claims description 67
239000000203 mixture Substances 0.000 claims description 60
150000001875 compounds Chemical class 0.000 claims description 58
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 54
229910052757 nitrogen Inorganic materials 0.000 claims description 49
150000003839 salts Chemical class 0.000 claims description 46
229910052717 sulfur Chemical group 0.000 claims description 44
229910052736 halogen Inorganic materials 0.000 claims description 42
125000005842 heteroatom Chemical group 0.000 claims description 42
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 42
150000002148 esters Chemical class 0.000 claims description 39
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 37
239000011593 sulfur Chemical group 0.000 claims description 37
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 35
229910052760 oxygen Inorganic materials 0.000 claims description 35
239000001301 oxygen Chemical group 0.000 claims description 35
125000004093 cyano group Chemical group *C#N 0.000 claims description 34
150000002367 halogens Chemical class 0.000 claims description 33
125000000753 cycloalkyl group Chemical group 0.000 claims description 30
230000000694 effects Effects 0.000 claims description 30
125000005843 halogen group Chemical group 0.000 claims description 29
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 27
238000009472 formulation Methods 0.000 claims description 23
125000004414 alkyl thio group Chemical group 0.000 claims description 21
125000006413 ring segment Chemical group 0.000 claims description 21
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 20
125000003545 alkoxy group Chemical group 0.000 claims description 18
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 18
125000003118 aryl group Chemical group 0.000 claims description 18
125000000623 heterocyclic group Chemical group 0.000 claims description 18
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
125000003282 alkyl amino group Chemical group 0.000 claims description 16
244000038559 crop plants Species 0.000 claims description 14
125000004663 dialkyl amino group Chemical group 0.000 claims description 14
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
125000005844 heterocyclyloxy group Chemical group 0.000 claims description 12
125000004433 nitrogen atom Chemical group N* 0.000 claims description 12
229930195733 hydrocarbon Natural products 0.000 claims description 11
229910052739 hydrogen Inorganic materials 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 11
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 10
239000004215 Carbon black (E152) Substances 0.000 claims description 10
RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical compound N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 claims description 9
125000004430 oxygen atom Chemical group O* 0.000 claims description 9
ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 9
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 8
125000002015 acyclic group Chemical group 0.000 claims description 8
125000004419 alkynylene group Chemical group 0.000 claims description 8
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 8
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 8
125000004450 alkenylene group Chemical group 0.000 claims description 7
125000004434 sulfur atom Chemical group 0.000 claims description 7
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 6
239000005531 Flufenacet Substances 0.000 claims description 6
125000002252 acyl group Chemical group 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 6
125000003302 alkenyloxy group Chemical group 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
125000002837 carbocyclic group Chemical group 0.000 claims description 6
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 claims description 6
125000001188 haloalkyl group Chemical group 0.000 claims description 6
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims description 6
125000004043 oxo group Chemical group O=* 0.000 claims description 6
125000006763 (C3-C9) cycloalkyl group Chemical group 0.000 claims description 5
239000005562 Glyphosate Substances 0.000 claims description 5
239000000654 additive Substances 0.000 claims description 5
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 5
125000003277 amino group Chemical group 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 5
230000008569 process Effects 0.000 claims description 5
238000009331 sowing Methods 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 4
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 4
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 4
125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 4
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
125000006805 (C3-C9) cycloalkylamino group Chemical group 0.000 claims description 4
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
239000005499 Clomazone Substances 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000005583 Metribuzin Substances 0.000 claims description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
125000004429 atom Chemical group 0.000 claims description 4
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 claims description 4
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 4
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 4
125000004122 cyclic group Chemical group 0.000 claims description 4
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 claims description 4
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
125000004468 heterocyclylthio group Chemical group 0.000 claims description 4
QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 claims description 4
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical class NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 claims description 3
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 3
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 claims description 3
239000003666 Amidosulfuron Substances 0.000 claims description 3
CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 3
NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 claims description 3
239000005489 Bromoxynil Substances 0.000 claims description 3
239000005492 Carfentrazone-ethyl Substances 0.000 claims description 3
239000005500 Clopyralid Substances 0.000 claims description 3
UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 claims description 3
239000005529 Florasulam Substances 0.000 claims 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 claims description 3
239000005559 Flurtamone Substances 0.000 claims description 3
239000005571 Isoxaflutole Substances 0.000 claims description 3
NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical group C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 claims description 3
MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 claims description 3
229940097068 glyphosate Drugs 0.000 claims description 3
125000004438 haloalkoxy group Chemical group 0.000 claims description 3
OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 claims description 3
229940088649 isoxaflutole Drugs 0.000 claims description 3
NWBNORAVIXIZTL-UHFFFAOYSA-N nitro thiocyanate Chemical compound [O-][N+](=O)SC#N NWBNORAVIXIZTL-UHFFFAOYSA-N 0.000 claims description 3
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 claims description 3
ROBSGBGTWRRYSK-SNVBAGLBSA-N (2r)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CC=C(C#N)C=C1F ROBSGBGTWRRYSK-SNVBAGLBSA-N 0.000 claims description 2
125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims description 2
125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 2
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 2
125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 2
125000005862 (C1-C6)alkanoyl group Chemical group 0.000 claims description 2
125000006768 (C3-C9) cycloalkoxy group Chemical group 0.000 claims description 2
OVXMBIVWNJDDSM-UHFFFAOYSA-N (benzhydrylideneamino) 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(=O)ON=C(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 OVXMBIVWNJDDSM-UHFFFAOYSA-N 0.000 claims description 2
RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 claims description 2
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 2
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 claims description 2
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 claims description 2
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 claims description 2
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 claims 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 claims description 2
IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims description 2
CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 claims description 2
ZBMRKNMTMPPMMK-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid;azane Chemical compound [NH4+].CP(O)(=O)CCC(N)C([O-])=O ZBMRKNMTMPPMMK-UHFFFAOYSA-N 0.000 claims description 2
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 claims description 2
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 2
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 2
239000005469 Azimsulfuron Substances 0.000 claims description 2
QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 claims description 2
PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims description 2
239000005472 Bensulfuron methyl Substances 0.000 claims description 2
239000005476 Bentazone Substances 0.000 claims description 2
239000005484 Bifenox Substances 0.000 claims description 2
239000005488 Bispyribac Substances 0.000 claims description 2
125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 2
239000005494 Chlorotoluron Substances 0.000 claims description 2
WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 claims description 2
239000005497 Clethodim Substances 0.000 claims description 2
OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 0.000 claims description 2
239000005501 Cycloxydim Substances 0.000 claims description 2
239000005504 Dicamba Substances 0.000 claims description 2
YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 claims description 2
239000005510 Diuron Substances 0.000 claims description 2
BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 claims description 2
PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
239000005530 Fluazifop-P Substances 0.000 claims description 2
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230000000149 penetrating effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003090 pesticide formulation Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000004476 plant protection product Substances 0.000 description 1
239000013612 plasmid Substances 0.000 description 1
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
230000006798 recombination Effects 0.000 description 1
238000005215 recombination Methods 0.000 description 1
108091092562 ribozyme Proteins 0.000 description 1
230000002786 root growth Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
239000004550 soluble concentrate Substances 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
231100000765 toxin Toxicity 0.000 description 1
108700012359 toxins Proteins 0.000 description 1
238000009966 trimming Methods 0.000 description 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 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
239000004552 water soluble powder Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/06—Nitrogen directly attached to an aromatic 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)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

SK377-2001A 1998-09-18 1999-09-20 Kombinácia herbicídov, spôsob ničenia škodlivých rastlín a použitie kombinácií herbicídov na ničenie škodlivých rastlín SK287091B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19842894A DE19842894A1 (de)	1998-09-18	1998-09-18	Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen in Nutzpflanzenkulturen
PCT/EP1999/006937 WO2000016627A1 (de)	1998-09-18	1999-09-20	Synergistische wirkstoffkombinationen zur bekämpfung von schadpflanzen

Publications (2)

Publication Number	Publication Date
SK3772001A3 SK3772001A3 (en)	2001-09-11
SK287091B6 true SK287091B6 (sk)	2009-11-05

Family

ID=7881466

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK377-2001A SK287091B6 (sk)	1998-09-18	1999-09-20	Kombinácia herbicídov, spôsob ničenia škodlivých rastlín a použitie kombinácií herbicídov na ničenie škodlivých rastlín

Country Status (26)

Country	Link
US (1)	US20040171489A1 (zh)
EP (1)	EP1113720B1 (zh)
JP (1)	JP4733269B2 (zh)
KR (1)	KR100676018B1 (zh)
CN (1)	CN1243477C (zh)
AT (1)	ATE315336T1 (zh)
AU (1)	AU772607B2 (zh)
BG (1)	BG65251B1 (zh)
BR (2)	BRPI9914496B1 (zh)
CA (1)	CA2344394A1 (zh)
CZ (1)	CZ303507B6 (zh)
DE (2)	DE19842894A1 (zh)
ES (1)	ES2257099T3 (zh)
HR (1)	HRP20010193B1 (zh)
HU (1)	HU229822B1 (zh)
ID (1)	ID29884A (zh)
IL (2)	IL142032A0 (zh)
NZ (1)	NZ510192A (zh)
PL (1)	PL200240B1 (zh)
PT (1)	PT1113720E (zh)
RU (1)	RU2261598C9 (zh)
SK (1)	SK287091B6 (zh)
TR (1)	TR200100781T2 (zh)
UA (1)	UA72746C2 (zh)
WO (1)	WO2000016627A1 (zh)
ZA (1)	ZA200102106B (zh)

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DE19960684A1 (de) *	1999-12-15	2001-06-21	Aventis Cropscience Gmbh	Kombinationen von herbiziden Alkylazinen und Safenern
GB0022835D0 (en)	2000-09-18	2000-11-01	Aventis Cropscience Sa	New herbicidal composition
GB0022932D0 (en)	2000-09-18	2000-11-01	Aventis Cropscience Sa	New herbicidal composition
GB0022833D0 (en)	2000-09-18	2000-11-01	Aventis Cropscience Sa	New herbicidal composition
DE10117505A1 (de) *	2001-04-07	2002-10-10	Bayer Cropscience Gmbh	Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen
DE10209468A1 (de) *	2002-03-05	2003-09-18	Bayer Cropscience Gmbh	Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen
DE10209430A1 (de)	2002-03-05	2003-09-18	Bayer Cropscience Gmbh	Herbizid-Kombination mit acylierten Aminophenylsulfonylharnstoffen
DE102004034571A1 (de) *	2004-07-17	2006-02-23	Bayer Cropscience Gmbh	Herbizide Mittel
EP1790227A1 (de)	2005-11-25	2007-05-30	Bayer CropScience AG	Wässrige Suspensionskonzentrate aus 2,4-Diamino-s-triazinherbiziden
EP1854355A1 (de) *	2006-03-15	2007-11-14	Bayer CropScience AG	Wässrige Suspensionskonzentrate
EP1958509A1 (de) *	2007-02-19	2008-08-20	Bayer CropScience AG	Herbizid-Kombination
WO2009089165A2 (en) *	2008-01-07	2009-07-16	Auburn University	Combinations of herbicides and safeners
CN102026545A (zh) *	2008-02-12	2011-04-20	北美爱利思达生命科学有限责任公司	控制多余植物的方法
EP2092825A1 (de) *	2008-02-21	2009-08-26	Bayer CropScience Aktiengesellschaft	Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine
AU2011218123B2 (en)	2010-02-19	2015-02-12	Corteva Agriscience Llc	Synergistic herbicide/fungicide composition containing a pyridine carboxylic acid and a fungicide
CA2803687C (en)	2010-07-20	2019-04-30	Vestaron Corporation	Insecticidal triazines and pyrimidines
CN101926349A (zh) *	2010-09-13	2010-12-29	尹小根	一组含有酰嘧磺隆与莠去津的除草组合物
US8916183B2 (en) *	2012-02-02	2014-12-23	Dow Agrosciences, Llc.	Pesticidal compositions and processes related thereto
US8916499B2 (en)	2012-07-24	2014-12-23	Dow Agrosciences, Llc.	Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and a protoporphyrinogen oxidase inhibitor
CN102986706B (zh) *	2012-12-20	2014-02-26	联保作物科技有限公司	一种水稻田除草组合物
AU2015250895B2 (en) *	2014-04-23	2018-11-01	Basf Se	Herbicidal combination comprising azines
AU2016254233B2 (en)	2015-04-27	2020-10-08	Basf Se	Herbicide combinations comprising glufosinate and indaziflam
BR112017024174B1 (pt)	2015-05-11	2023-01-10	Basf Se	Combinações de herbicida que compreendem l-glufosinato e indaziflam
MX2021009954A (es)	2019-02-19	2021-12-10	Gowan Company L L C	Composiciones liquidas estables y metodos para usar las mismas.
KR20230038457A (ko)	2020-06-10	2023-03-20	알리고스 테라퓨틱스 인코포레이티드	코로나바이러스, 피코르나바이러스 및 노로바이러스 감염을 치료하기 위한 항바이러스 화합물
IL309732A (en)	2021-07-09	2024-02-01	Aligos Therapeutics Inc	Antiviral compounds

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JPH0489409A (ja) *	1990-08-01	1992-03-23	Idemitsu Kosan Co Ltd	除草剤組成物
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DE19607450A1 (de) *	1996-02-28	1997-09-04	Hoechst Schering Agrevo Gmbh	2-Amino-4-bicycloamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
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DE19641692A1 (de) *	1996-10-10	1998-04-23	Bayer Ag	Substituierte 2,4-Diamino-1,3,5-triazine
DE19641694A1 (de) *	1996-10-10	1998-04-16	Bayer Ag	Substituierte 2,4-Diamino-1,3,5-triazine
DE19641693A1 (de) *	1996-10-10	1998-04-16	Bayer Ag	Substituierte 2-Amino-4-alkylamino-1,3,5-triazine
DE19641691A1 (de) *	1996-10-10	1998-04-16	Bayer Ag	Substituierte 2-Amino-4-alkylamino-1,3,5-triazine
DE19704922A1 (de) *	1997-02-10	1998-08-13	Hoechst Schering Agrevo Gmbh	2,4-Diamino-1,3,5-triazine, ihre Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DE19711825A1 (de) *	1997-03-21	1998-09-24	Bayer Ag	Substituierte 2,4-Diamino-1,3,5-triazine
DE19744232A1 (de) *	1997-10-07	1999-04-08	Bayer Ag	Substituierte 2,4-Diamino-1,3,5-triazine
DE19744711A1 (de) *	1997-10-10	1999-04-15	Bayer Ag	Substituierte 2,4-Diamino-1,3,5-triazine
DE19802236A1 (de) *	1998-01-22	1999-07-29	Bayer Ag	Substituierte Aminoalkylidenaminotriazine
DE19925329A1 (de) *	1998-06-16	1999-12-23	Hoechst Schering Agrevo Gmbh	2,4-Diamino-1,3,5-triazine, Verfahren zur Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DE19828519A1 (de) *	1998-06-26	1999-12-30	Hoechst Schering Agrevo Gmbh	Substituierte 2,4-Diamino-1,3,5-triazine, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren

1998
- 1998-09-18 DE DE19842894A patent/DE19842894A1/de not_active Withdrawn
1999
- 1999-09-20 AU AU59796/99A patent/AU772607B2/en not_active Expired
- 1999-09-20 ID IDW20010614A patent/ID29884A/id unknown
- 1999-09-20 SK SK377-2001A patent/SK287091B6/sk not_active IP Right Cessation
- 1999-09-20 PT PT99969311T patent/PT1113720E/pt unknown
- 1999-09-20 KR KR1020017003489A patent/KR100676018B1/ko active IP Right Grant
- 1999-09-20 NZ NZ510192A patent/NZ510192A/en not_active IP Right Cessation
- 1999-09-20 UA UA2001042577A patent/UA72746C2/uk unknown
- 1999-09-20 WO PCT/EP1999/006937 patent/WO2000016627A1/de active IP Right Grant
- 1999-09-20 CA CA002344394A patent/CA2344394A1/en not_active Abandoned
- 1999-09-20 RU RU2001107142/04A patent/RU2261598C9/ru active
- 1999-09-20 CZ CZ20010986A patent/CZ303507B6/cs not_active IP Right Cessation
- 1999-09-20 PL PL346878A patent/PL200240B1/pl unknown
- 1999-09-20 IL IL14203299A patent/IL142032A0/xx active IP Right Grant
- 1999-09-20 CN CNB99811054XA patent/CN1243477C/zh not_active Expired - Lifetime
- 1999-09-20 DE DE59913050T patent/DE59913050D1/de not_active Expired - Lifetime
- 1999-09-20 BR BRPI9914496A patent/BRPI9914496B1/pt active IP Right Grant
- 1999-09-20 JP JP2000573598A patent/JP4733269B2/ja not_active Expired - Lifetime
- 1999-09-20 EP EP99969311A patent/EP1113720B1/de not_active Expired - Lifetime
- 1999-09-20 AT AT99969311T patent/ATE315336T1/de not_active IP Right Cessation
- 1999-09-20 BR BRPI9917835-4A patent/BR9917835B1/pt active IP Right Grant
- 1999-09-20 ES ES99969311T patent/ES2257099T3/es not_active Expired - Lifetime
- 1999-09-20 HU HU0104269A patent/HU229822B1/hu unknown
- 1999-09-20 TR TR2001/00781T patent/TR200100781T2/xx unknown
2001
- 2001-03-09 BG BG105324A patent/BG65251B1/bg unknown
- 2001-03-14 ZA ZA200102106A patent/ZA200102106B/en unknown
- 2001-03-15 HR HR20010193A patent/HRP20010193B1/xx not_active IP Right Cessation
- 2001-03-15 IL IL142032A patent/IL142032A/en not_active IP Right Cessation
2003
- 2003-12-12 US US10/734,792 patent/US20040171489A1/en not_active Abandoned

Also Published As

Publication number	Publication date
WO2000016627A1 (de)	2000-03-30
AU772607B2 (en)	2004-05-06
PL200240B1 (pl)	2008-12-31
RU2261598C9 (ru)	2006-03-27
TR200100781T2 (tr)	2001-10-22
AU5979699A (en)	2000-04-10
CN1243477C (zh)	2006-03-01
HRP20010193B1 (en)	2010-10-31
ATE315336T1 (de)	2006-02-15
KR20010085820A (ko)	2001-09-07
BG65251B1 (bg)	2007-10-31
PT1113720E (pt)	2006-05-31
NZ510192A (en)	2003-12-19
EP1113720A1 (de)	2001-07-11
ES2257099T3 (es)	2006-07-16
HUP0104269A2 (hu)	2002-03-28
CZ303507B6 (cs)	2012-10-31
CZ2001986A3 (cs)	2001-07-11
BR9917835B1 (pt)	2013-03-19
JP4733269B2 (ja)	2011-07-27
EP1113720B1 (de)	2006-01-11
DE59913050D1 (de)	2006-04-06
KR100676018B1 (ko)	2007-01-29
ID29884A (id)	2001-10-18
IL142032A0 (en)	2002-03-10
BR9914496A (pt)	2001-06-26
CA2344394A1 (en)	2000-03-30
IL142032A (en)	2006-08-20
DE19842894A1 (de)	2000-03-23
US20040171489A1 (en)	2004-09-02
JP2002526428A (ja)	2002-08-20
BG105324A (bg)	2001-12-29
UA72746C2 (en)	2005-04-15
HUP0104269A3 (en)	2002-04-29
PL346878A1 (en)	2002-03-11
RU2261598C2 (ru)	2005-10-10
HU229822B1 (en)	2014-08-28
CN1317931A (zh)	2001-10-17
HRP20010193A2 (en)	2002-04-30
BRPI9914496B1 (pt)	2016-08-16
SK3772001A3 (en)	2001-09-11
ZA200102106B (en)	2002-10-14

Legal Events

Date

Code

Title

Description

2016-02-02

PC4A

Assignment and transfer of rights

Owner name: BAYER INTELLECTUAL PROPERTY GMBH, MONHEIM AM R, DE

Free format text: FORMER OWNER: BAYER CROPSCIENCE AKTIENGESELLSCHAFT, MONHEIM, DE

Effective date: 20151006

2019-11-05

MK4A

Patent expired

Expiry date: 20190920

Publication	Publication Date	Title
SK287091B6 (sk)	2009-11-05	Kombinácia herbicídov, spôsob ničenia škodlivých rastlín a použitie kombinácií herbicídov na ničenie škodlivých rastlín
JP5974072B2 (ja)	2016-08-23	ジメトキシトリアジニル置換ジフルオロメタンスルホニルアニリド類を含む除草剤組み合わせ
TW584542B (en)	2004-04-21	Herbicidal compositions with acylated aminophenylsulfonylureas
ES2447874T3 (es)	2014-03-13	Composición herbicida sinérgica que contiene ciertos ácidos carboxílicos de piridina y ciertos herbicidas de cereal y arroz
WO2000003591A2 (de)	2000-01-27	Herbizide mittel
KR101663102B1 (ko)	2016-10-14	디메톡시트리아지닐-치환 디플루오로메탄설포닐아닐리드를 포함하는 제초제 배합물
PL215315B1 (pl)	2013-11-29	Zastosowanie kompozycji zawierajacej glifosat i diflufenzopir, sposób zwalczania szkodliwych roslin w uprawach kukurydzy oraz kompozycja herbicydów
WO2000008935A1 (de)	2000-02-24	Herbizide mittel für tolerante oder resistente reiskulturen
KR101663097B1 (ko)	2016-10-14	디메톡시트리아지닐-치환 디플루오로메탄설포닐아닐리드를 포함하는 제초제 배합물
KR101663095B1 (ko)	2016-10-14	디메톡시트리아지닐-치환 디플루오로메탄설포닐아닐리드를 포함하는 제초제 배합물
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