DE19827855A1 - Kombinationen aus Herbiziden und Safenern - Google Patents
Kombinationen aus Herbiziden und SafenernInfo
- Publication number
- DE19827855A1 DE19827855A1 DE19827855A DE19827855A DE19827855A1 DE 19827855 A1 DE19827855 A1 DE 19827855A1 DE 19827855 A DE19827855 A DE 19827855A DE 19827855 A DE19827855 A DE 19827855A DE 19827855 A1 DE19827855 A1 DE 19827855A1
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- substituted
- alkoxy
- phenyl
- hydrogen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract description 52
- 239000004009 herbicide Substances 0.000 title abstract description 45
- 241000196324 Embryophyta Species 0.000 title description 41
- 235000013339 cereals Nutrition 0.000 title description 9
- 229920000742 Cotton Polymers 0.000 title description 3
- 244000068988 Glycine max Species 0.000 title description 3
- 235000010469 Glycine max Nutrition 0.000 title description 3
- -1 aryl ketone Chemical class 0.000 abstract description 97
- 239000000203 mixture Substances 0.000 abstract description 46
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 37
- 229910052760 oxygen Inorganic materials 0.000 abstract description 21
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 20
- 150000002148 esters Chemical class 0.000 abstract description 19
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract description 18
- 125000003342 alkenyl group Chemical group 0.000 abstract description 17
- 229910052717 sulfur Inorganic materials 0.000 abstract description 16
- 125000000304 alkynyl group Chemical group 0.000 abstract description 15
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 12
- 125000000217 alkyl group Chemical group 0.000 abstract description 11
- 125000003118 aryl group Chemical group 0.000 abstract description 11
- 150000003839 salts Chemical class 0.000 abstract description 11
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract description 10
- 125000005842 heteroatom Chemical group 0.000 abstract description 10
- 229920006395 saturated elastomer Polymers 0.000 abstract description 10
- 239000002253 acid Substances 0.000 abstract description 8
- 125000000262 haloalkenyl group Chemical group 0.000 abstract description 8
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 abstract description 7
- 239000002794 2,4-DB Substances 0.000 abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 abstract description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 7
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract description 7
- 125000001424 substituent group Chemical group 0.000 abstract description 7
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract description 6
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 abstract description 6
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 abstract description 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract description 6
- 229910052799 carbon Inorganic materials 0.000 abstract description 6
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 abstract description 5
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract description 5
- 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 description 4
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract description 4
- 239000005504 Dicamba Substances 0.000 abstract description 4
- 239000005574 MCPA Substances 0.000 abstract description 4
- 239000005575 MCPB Substances 0.000 abstract description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract description 4
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract description 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract description 4
- 125000002541 furyl group Chemical group 0.000 abstract description 4
- 125000001544 thienyl group Chemical group 0.000 abstract description 4
- SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 abstract description 3
- PYKLUAIDKVVEOS-RAXLEYEMSA-N (e)-n-(cyanomethoxy)benzenecarboximidoyl cyanide Chemical compound N#CCO\N=C(\C#N)C1=CC=CC=C1 PYKLUAIDKVVEOS-RAXLEYEMSA-N 0.000 abstract description 3
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 abstract description 3
- AXHCGXRBOHBEQA-UHFFFAOYSA-N 2-(5-chloro-2-methylphenoxy)acetic acid Chemical compound CC1=CC=C(Cl)C=C1OCC(O)=O AXHCGXRBOHBEQA-UHFFFAOYSA-N 0.000 abstract description 3
- SIYAHZSHQIPQLY-UHFFFAOYSA-N 4-(4-chlorophenoxy)butanoic acid Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1 SIYAHZSHQIPQLY-UHFFFAOYSA-N 0.000 abstract description 3
- PYKLUAIDKVVEOS-UHFFFAOYSA-N Cyometrinil Chemical compound N#CCON=C(C#N)C1=CC=CC=C1 PYKLUAIDKVVEOS-UHFFFAOYSA-N 0.000 abstract description 3
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 abstract description 3
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 abstract description 3
- WFVUIONFJOAYPK-KAMYIIQDSA-N Oxabetrinil Chemical compound C=1C=CC=CC=1C(/C#N)=N\OCC1OCCO1 WFVUIONFJOAYPK-KAMYIIQDSA-N 0.000 abstract description 3
- 125000003302 alkenyloxy group Chemical group 0.000 abstract description 3
- 150000001408 amides Chemical class 0.000 abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 3
- JCHMGYRXQDASJE-UHFFFAOYSA-N metcamifen Chemical compound C1=CC(NC(=O)NC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1OC JCHMGYRXQDASJE-UHFFFAOYSA-N 0.000 abstract description 3
- LQPRNRFJJUSONA-UHFFFAOYSA-N methyl 2-benzhydryloxyacetate Chemical compound C=1C=CC=CC=1C(OCC(=O)OC)C1=CC=CC=C1 LQPRNRFJJUSONA-UHFFFAOYSA-N 0.000 abstract description 3
- WFVUIONFJOAYPK-UHFFFAOYSA-N n-(1,3-dioxolan-2-ylmethoxy)benzenecarboximidoyl cyanide Chemical compound C=1C=CC=CC=1C(C#N)=NOCC1OCCO1 WFVUIONFJOAYPK-UHFFFAOYSA-N 0.000 abstract description 3
- ZYAOTFVRVOXVSD-UHFFFAOYSA-N n-[4-(dimethylcarbamoylamino)phenyl]sulfonylnaphthalene-1-carboxamide Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC2=CC=CC=C12 ZYAOTFVRVOXVSD-UHFFFAOYSA-N 0.000 abstract description 3
- 125000000335 thiazolyl group Chemical group 0.000 abstract description 3
- 150000001412 amines Chemical class 0.000 abstract description 2
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 abstract description 2
- NYDKNJDNBUFWRJ-UHFFFAOYSA-N n-[4-(dimethylcarbamoylamino)phenyl]sulfonyl-2-methoxybenzamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(NC(=O)N(C)C)C=C1 NYDKNJDNBUFWRJ-UHFFFAOYSA-N 0.000 abstract description 2
- 125000005936 piperidyl group Chemical group 0.000 abstract description 2
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 4
- 125000000565 sulfonamide group Chemical group 0.000 abstract 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 150000003997 cyclic ketones Chemical class 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- SJWOCKTZFQIKHZ-UHFFFAOYSA-N (1-ethoxy-1-oxopropan-2-yl) 3,6-dichloro-2-methoxybenzoate Chemical compound CCOC(=O)C(C)OC(=O)C1=C(Cl)C=CC(Cl)=C1OC SJWOCKTZFQIKHZ-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- QECVIPBZOPUTRD-UHFFFAOYSA-N N=S(=O)=O Chemical class N=S(=O)=O QECVIPBZOPUTRD-UHFFFAOYSA-N 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical group O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 abstract 1
- 150000002466 imines Chemical class 0.000 abstract 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 abstract 1
- 150000003248 quinolines Chemical class 0.000 abstract 1
- 125000006168 tricyclic group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 106
- 150000003254 radicals Chemical class 0.000 description 69
- 229910052739 hydrogen Inorganic materials 0.000 description 64
- 239000001257 hydrogen Substances 0.000 description 63
- 150000001875 compounds Chemical class 0.000 description 61
- 229910052736 halogen Inorganic materials 0.000 description 59
- 150000002367 halogens Chemical class 0.000 description 50
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 46
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 36
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 32
- 239000004480 active ingredient Substances 0.000 description 32
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 23
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 19
- 238000009472 formulation Methods 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 17
- 150000002431 hydrogen Chemical class 0.000 description 16
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 15
- 125000004414 alkyl thio group Chemical group 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 240000007594 Oryza sativa Species 0.000 description 14
- 239000008187 granular material Substances 0.000 description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 14
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 13
- 235000007164 Oryza sativa Nutrition 0.000 description 13
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 13
- 235000009566 rice Nutrition 0.000 description 13
- 125000004093 cyano group Chemical group *C#N 0.000 description 12
- 230000009931 harmful effect Effects 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 229910052731 fluorine Inorganic materials 0.000 description 10
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 9
- 240000008042 Zea mays Species 0.000 description 9
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 8
- 230000009261 transgenic effect Effects 0.000 description 8
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 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 description 7
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 7
- 235000005822 corn Nutrition 0.000 description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 125000005103 alkyl silyl group Chemical group 0.000 description 6
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 125000006413 ring segment Chemical group 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 239000004562 water dispersible granule Substances 0.000 description 6
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 240000005979 Hordeum vulgare Species 0.000 description 5
- 235000007340 Hordeum vulgare Nutrition 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 239000000729 antidote Substances 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 229920000151 polyglycol Polymers 0.000 description 5
- 239000010695 polyglycol Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 244000038559 crop plants Species 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 125000004995 haloalkylthio group Chemical group 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 230000000885 phytotoxic effect Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 description 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 3
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 description 3
- 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 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229910004013 NO 2 Inorganic materials 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 3
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 description 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 3
- 125000003282 alkyl amino group Chemical group 0.000 description 3
- 125000005277 alkyl imino group Chemical group 0.000 description 3
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 125000004663 dialkyl amino group Chemical group 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 125000004438 haloalkoxy group Chemical group 0.000 description 3
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 3
- 125000001072 heteroaryl group Chemical group 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000003621 irrigation water Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- 125000002950 monocyclic group Chemical group 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 3
- 239000011814 protection agent Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 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 description 2
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- 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 2
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- 125000001425 triazolyl group Chemical group 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical compound COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/18—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with sulfur as the ring hetero atom
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/80—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Priority Applications (26)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19827855A DE19827855A1 (de) | 1998-06-23 | 1998-06-23 | Kombinationen aus Herbiziden und Safenern |
| MXPA01000081 MX231281B (es) | 1998-06-23 | 1999-06-09 | Combinaciones de herbicidas y antidotos. |
| HU0103422A HU230076B1 (hu) | 1998-06-23 | 1999-06-09 | Gyomirtó szert és antidótumot tartalmazó kombináció |
| EP04002856A EP1415537B1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus Herbiziden und Safenern |
| CA002335945A CA2335945C (en) | 1998-06-23 | 1999-06-09 | Combinations of herbicides and safeners |
| CNB99807747XA CN1167340C (zh) | 1998-06-23 | 1999-06-09 | 除草剂与安全剂的组合 |
| AU45104/99A AU4510499A (en) | 1998-06-23 | 1999-06-09 | Combination of herbicides and safeners |
| BRPI9911443-7A BR9911443B1 (pt) | 1998-06-23 | 1999-06-09 | composição herbicidamente ativa e processo para combate de plantas daninhas. |
| JP2000555495A JP4653307B2 (ja) | 1998-06-23 | 1999-06-09 | 除草剤と毒性緩和剤の結合 |
| ES99927934T ES2229720T3 (es) | 1998-06-23 | 1999-06-09 | Combinaciones de herbicidas y antidotos. |
| DE59910460T DE59910460D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus herbiziden und safenern |
| BRPI9917879-6A BR9917879B1 (pt) | 1998-06-23 | 1999-06-09 | composição herbicidamente ativa e processo para combate de plantas daninhas. |
| RU2001101986/04A RU2221427C2 (ru) | 1998-06-23 | 1999-06-09 | Комбинации гербицидов и протекторов, способ борьбы с сорными растениями |
| KR1020007014753A KR20010053176A (ko) | 1998-06-23 | 1999-06-09 | 제초제와 완화제의 조합물 |
| PCT/EP1999/003980 WO1999066795A1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus herbiziden und safenern |
| DE59915101T DE59915101D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus Herbiziden und Safenern |
| MXPA03008633 MX240911B (es) | 1998-06-23 | 1999-06-09 | Combinaciones de herbicidas y protectores. |
| HU1500132A HU230493B1 (hu) | 1998-06-23 | 1999-06-09 | Gyomirtó szert és antidótumot tartalmazó kombináció |
| ES04002856T ES2334441T3 (es) | 1998-06-23 | 1999-06-09 | Combinaciones de herbicidas y antidotos. |
| EP99927934A EP1089627B1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus herbiziden und safenern |
| ARP990102944A AR019870A1 (es) | 1998-06-23 | 1999-06-18 | Agente activo como herbicida y procedimiento para reprimir plantas daninas en cultivos. |
| US09/337,135 US6511940B1 (en) | 1998-06-23 | 1999-06-21 | Combination of herbicides and safeners |
| TW88110359A TW574024B (en) | 1998-06-23 | 1999-06-21 | Combinations of herbicides and safeners |
| PH11999001531A PH11999001531B1 (en) | 1998-06-23 | 1999-06-22 | Combination of herbicides and safeners |
| ZA200007302A ZA200007302B (en) | 1998-06-23 | 2000-12-08 | Combination of herbicides and safeners. |
| US10/265,925 US7135434B2 (en) | 1998-06-23 | 2002-10-07 | Combinations of herbicides and safeners |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19827855A DE19827855A1 (de) | 1998-06-23 | 1998-06-23 | Kombinationen aus Herbiziden und Safenern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE19827855A1 true DE19827855A1 (de) | 1999-12-30 |
Family
ID=7871700
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19827855A Withdrawn DE19827855A1 (de) | 1998-06-23 | 1998-06-23 | Kombinationen aus Herbiziden und Safenern |
| DE59915101T Expired - Lifetime DE59915101D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus Herbiziden und Safenern |
| DE59910460T Expired - Fee Related DE59910460D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus herbiziden und safenern |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE59915101T Expired - Lifetime DE59915101D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus Herbiziden und Safenern |
| DE59910460T Expired - Fee Related DE59910460D1 (de) | 1998-06-23 | 1999-06-09 | Kombinationen aus herbiziden und safenern |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US6511940B1 (enExample) |
| EP (2) | EP1089627B1 (enExample) |
| JP (1) | JP4653307B2 (enExample) |
| KR (1) | KR20010053176A (enExample) |
| CN (1) | CN1167340C (enExample) |
| AR (1) | AR019870A1 (enExample) |
| AU (1) | AU4510499A (enExample) |
| BR (2) | BR9917879B1 (enExample) |
| CA (1) | CA2335945C (enExample) |
| DE (3) | DE19827855A1 (enExample) |
| ES (2) | ES2229720T3 (enExample) |
| HU (2) | HU230076B1 (enExample) |
| MX (2) | MX231281B (enExample) |
| PH (1) | PH11999001531B1 (enExample) |
| RU (1) | RU2221427C2 (enExample) |
| TW (1) | TW574024B (enExample) |
| WO (1) | WO1999066795A1 (enExample) |
| ZA (1) | ZA200007302B (enExample) |
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| WO2002015695A3 (en) * | 2000-08-25 | 2002-06-13 | Basf Ag | Synergistic combination of a dihydrobenzothiophene herbicide and a photosystem ii inhibitor |
| US6750230B2 (en) | 2000-07-07 | 2004-06-15 | Pfizer, Inc. | Pyrazole derivatives |
| DE10351234A1 (de) * | 2003-11-03 | 2005-06-16 | Bayer Cropscience Gmbh | Herbizid wirksames Mittel |
| DE10355846A1 (de) * | 2003-11-26 | 2005-07-07 | Bayer Cropscience Gmbh | Herbizid wirksames Mittel |
| US7432226B2 (en) | 2003-11-03 | 2008-10-07 | Bayer Cropscience Gmbh | Herbicidally active composition |
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| DE19853827A1 (de) * | 1998-11-21 | 2000-05-25 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| DE19936437A1 (de) * | 1999-08-03 | 2001-02-08 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| HU230234B1 (hu) * | 1999-09-08 | 2015-10-28 | Aventis Cropscience Uk Ltd. | Új herbicid készítmények |
| DE19950943A1 (de) * | 1999-10-22 | 2001-05-17 | Aventis Cropscience Gmbh | Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Hemmstoffe der Hydroxyphenylpyruvat-Dioxygenase |
| DE19958381A1 (de) * | 1999-12-03 | 2001-06-07 | Bayer Ag | Herbizide auf Basis von N-Aryl-uracilen |
| DE10031825A1 (de) * | 2000-06-30 | 2002-01-10 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
| US20040110637A1 (en) * | 2001-01-31 | 2004-06-10 | Frank Ziemer | Method of safening crops using isoxazoline carboxylates |
| DE10106420A1 (de) * | 2001-02-12 | 2002-08-14 | Bayer Ag | Selektive Herbizide auf Basis von substituierten Arylketonen und Safenern |
| DE10119721A1 (de) * | 2001-04-21 | 2002-10-31 | Bayer Cropscience Gmbh | Herbizide Mittel enthaltend Benzoylcyclohexandione und Safener |
| DE10127328A1 (de) | 2001-06-06 | 2002-12-19 | Bayer Cropscience Gmbh | Herbizide Mittel enthaltend Benzoylpyrazole und Safener |
| DE10142333A1 (de) * | 2001-08-30 | 2003-03-20 | Bayer Cropscience Ag | Herbizide Mischungen auf Basis von substituierten Arylketonen |
| DE10142334A1 (de) * | 2001-08-30 | 2003-03-20 | Bayer Cropscience Ag | Herbizide auf Basis von substituierten Arylketonen |
| DE10143083A1 (de) * | 2001-09-03 | 2003-03-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten Arylsulfonylaminocarbonyltriazolinonen und Safenern |
| DE10145019A1 (de) * | 2001-09-13 | 2003-04-03 | Bayer Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| DE10146590A1 (de) | 2001-09-21 | 2003-04-10 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern |
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| DE4440354A1 (de) * | 1994-11-11 | 1996-05-15 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Phenylsulfonylharnstoff-Herbiziden und Safenern |
| US5627131A (en) * | 1995-01-09 | 1997-05-06 | Zeneca Limited | Herbicidal compositions of 4-benzoylisoxazole and antidotes therefor |
| WO1996025413A1 (fr) * | 1995-02-15 | 1996-08-22 | Idemitsu Kosan Co., Ltd. | Derives d'isoxazole |
| CZ293254B6 (cs) * | 1995-02-24 | 2004-03-17 | Basf Aktiengesellschaft | Pyrazolylbenzoylový derivát, způsob jeho přípravy, herbicidní prostředek s jeho obsahem a způsob potírání nežádoucích rostlin |
| PL324318A1 (en) * | 1995-06-29 | 1998-05-25 | Du Pont | Herbicidal ketals and spirocyclic compounds |
| WO1997013765A1 (en) * | 1995-10-09 | 1997-04-17 | Idemitsu Kosan Co., Ltd. | 2-cyano-1,3-dione derivatives and herbicides containing the same as active ingredient |
| GB9606015D0 (en) * | 1996-03-22 | 1996-05-22 | Rhone Poulenc Agriculture | New herbicides |
| DE19621522A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| DE19742951A1 (de) * | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| WO2000017194A1 (en) * | 1998-05-22 | 2000-03-30 | Dow Agrosciences Llc | 1-alkyl-4-[(3-oxetanyl-)benzoyl]-5-hydroxypyrazole compounds and their use as herbicides |
-
1998
- 1998-06-23 DE DE19827855A patent/DE19827855A1/de not_active Withdrawn
-
1999
- 1999-06-09 JP JP2000555495A patent/JP4653307B2/ja not_active Expired - Lifetime
- 1999-06-09 BR BRPI9917879-6A patent/BR9917879B1/pt not_active IP Right Cessation
- 1999-06-09 WO PCT/EP1999/003980 patent/WO1999066795A1/de not_active Ceased
- 1999-06-09 ES ES99927934T patent/ES2229720T3/es not_active Expired - Lifetime
- 1999-06-09 ES ES04002856T patent/ES2334441T3/es not_active Expired - Lifetime
- 1999-06-09 CN CNB99807747XA patent/CN1167340C/zh not_active Expired - Lifetime
- 1999-06-09 HU HU0103422A patent/HU230076B1/hu unknown
- 1999-06-09 MX MXPA01000081 patent/MX231281B/es active IP Right Grant
- 1999-06-09 DE DE59915101T patent/DE59915101D1/de not_active Expired - Lifetime
- 1999-06-09 EP EP99927934A patent/EP1089627B1/de not_active Expired - Lifetime
- 1999-06-09 CA CA002335945A patent/CA2335945C/en not_active Expired - Lifetime
- 1999-06-09 AU AU45104/99A patent/AU4510499A/en not_active Abandoned
- 1999-06-09 EP EP04002856A patent/EP1415537B1/de not_active Expired - Lifetime
- 1999-06-09 KR KR1020007014753A patent/KR20010053176A/ko not_active Ceased
- 1999-06-09 MX MXPA03008633 patent/MX240911B/es unknown
- 1999-06-09 RU RU2001101986/04A patent/RU2221427C2/ru active
- 1999-06-09 HU HU1500132A patent/HU230493B1/hu unknown
- 1999-06-09 DE DE59910460T patent/DE59910460D1/de not_active Expired - Fee Related
- 1999-06-09 BR BRPI9911443-7A patent/BR9911443B1/pt not_active IP Right Cessation
- 1999-06-18 AR ARP990102944A patent/AR019870A1/es active IP Right Grant
- 1999-06-21 US US09/337,135 patent/US6511940B1/en not_active Expired - Lifetime
- 1999-06-21 TW TW88110359A patent/TW574024B/zh active
- 1999-06-22 PH PH11999001531A patent/PH11999001531B1/en unknown
-
2000
- 2000-12-08 ZA ZA200007302A patent/ZA200007302B/en unknown
-
2002
- 2002-10-07 US US10/265,925 patent/US7135434B2/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6750230B2 (en) | 2000-07-07 | 2004-06-15 | Pfizer, Inc. | Pyrazole derivatives |
| US7141585B2 (en) | 2000-07-07 | 2006-11-28 | Agouron Pharmaceuticals, Inc. | Pyrazole derivatives |
| WO2002015695A3 (en) * | 2000-08-25 | 2002-06-13 | Basf Ag | Synergistic combination of a dihydrobenzothiophene herbicide and a photosystem ii inhibitor |
| DE10351234A1 (de) * | 2003-11-03 | 2005-06-16 | Bayer Cropscience Gmbh | Herbizid wirksames Mittel |
| US7432226B2 (en) | 2003-11-03 | 2008-10-07 | Bayer Cropscience Gmbh | Herbicidally active composition |
| DE10355846A1 (de) * | 2003-11-26 | 2005-07-07 | Bayer Cropscience Gmbh | Herbizid wirksames Mittel |
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| 8127 | New person/name/address of the applicant |
Owner name: AVENTIS CROPSCIENCE GMBH, 13509 BERLIN, DE |
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| 8127 | New person/name/address of the applicant |
Owner name: AVENTIS CROPSCIENCE GMBH, 65929 FRANKFURT, DE |
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| 8139 | Disposal/non-payment of the annual fee |