AP106A - Synergistic mixture - Google Patents
Synergistic mixture Download PDFInfo
- Publication number
- AP106A AP106A APAP/P/1989/000138A AP8900138A AP106A AP 106 A AP106 A AP 106A AP 8900138 A AP8900138 A AP 8900138A AP 106 A AP106 A AP 106A
- Authority
- AP
- ARIPO
- Prior art keywords
- chloroacetyl
- dimethylaniline
- methylaniline
- ethyl
- diethylaniline
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 70
- 230000002195 synergetic effect Effects 0.000 title description 14
- -1 1,3-dioxolan-2-yl Chemical group 0.000 claims abstract description 45
- 239000004480 active ingredient Substances 0.000 claims abstract description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 26
- 239000001257 hydrogen Substances 0.000 claims abstract description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 24
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 24
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 12
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- YTWKCBYYGUJDQD-UHFFFAOYSA-N 2-chloro-n-(cyclohexen-1-yl)acetamide Chemical compound ClCC(=O)NC1=CCCCC1 YTWKCBYYGUJDQD-UHFFFAOYSA-N 0.000 claims abstract description 8
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004509 1,3,4-oxadiazol-2-yl group Chemical group O1C(=NN=C1)* 0.000 claims abstract description 6
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims abstract description 6
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 6
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract description 6
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 6
- 125000006331 halo benzoyl group Chemical group 0.000 claims abstract description 5
- 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 claims abstract description 4
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 39
- 241000196324 Embryophyta Species 0.000 claims description 34
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 14
- 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 13
- 239000005977 Ethylene Substances 0.000 claims description 12
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 claims description 10
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 10
- 239000005580 Metazachlor Substances 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 244000045561 useful plants Species 0.000 claims description 5
- 244000068988 Glycine max Species 0.000 claims description 4
- 235000010469 Glycine max Nutrition 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- ZMFVLNREWBABDO-UHFFFAOYSA-N 2-chloro-n-propan-2-yl-n-(3,3,5,5-tetramethylcyclohexen-1-yl)acetamide Chemical compound ClCC(=O)N(C(C)C)C1=CC(C)(C)CC(C)(C)C1 ZMFVLNREWBABDO-UHFFFAOYSA-N 0.000 claims description 3
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 claims description 3
- 235000003276 Apios tuberosa Nutrition 0.000 claims description 3
- 235000010777 Arachis hypogaea Nutrition 0.000 claims description 3
- 235000010744 Arachis villosulicarpa Nutrition 0.000 claims description 3
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 3
- 244000299507 Gossypium hirsutum Species 0.000 claims description 3
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 3
- 240000007594 Oryza sativa Species 0.000 claims description 3
- 235000007164 Oryza sativa Nutrition 0.000 claims description 3
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims description 3
- 235000021536 Sugar beet Nutrition 0.000 claims description 3
- 240000008042 Zea mays Species 0.000 claims description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 3
- 125000000304 alkynyl group Chemical group 0.000 claims description 3
- 125000005336 allyloxy group Chemical group 0.000 claims description 3
- 235000009973 maize Nutrition 0.000 claims description 3
- QTGVGIVRLSGTJJ-UHFFFAOYSA-N n-(acetamidomethyl)-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(CNC(C)=O)C(=O)CCl QTGVGIVRLSGTJJ-UHFFFAOYSA-N 0.000 claims description 3
- 235000009566 rice Nutrition 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- BQSCJUWZCLCXJK-UHFFFAOYSA-N 2-chloro-n-(1,3-dioxan-2-ylmethyl)-n-(2-ethyl-6-methylphenyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(=O)CCl)CC1OCCCO1 BQSCJUWZCLCXJK-UHFFFAOYSA-N 0.000 claims description 2
- NXFSZAARYUBOBT-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(C(C)COC)C(=O)CCl NXFSZAARYUBOBT-UHFFFAOYSA-N 0.000 claims description 2
- STLBIPCVNZLGSV-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(2-methoxyethyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(CCOC)C(=O)CCl STLBIPCVNZLGSV-UHFFFAOYSA-N 0.000 claims description 2
- NIZACMDZBQKMTD-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(2-propoxyethyl)acetamide Chemical compound CCCOCCN(C(=O)CCl)C1=C(C)C=CC=C1C NIZACMDZBQKMTD-UHFFFAOYSA-N 0.000 claims description 2
- QOOIYASRVAOGIL-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-phenacylacetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CC(=O)C1=CC=CC=C1 QOOIYASRVAOGIL-UHFFFAOYSA-N 0.000 claims description 2
- QDOJXLUCPMRXBN-UHFFFAOYSA-N 2-chloro-n-(2-chloro-6-methylphenyl)-n-(2-ethoxyethyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(C)C=CC=C1Cl QDOJXLUCPMRXBN-UHFFFAOYSA-N 0.000 claims description 2
- GMDBXHNSCSJZLE-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(2-propoxyethyl)acetamide Chemical compound CCCOCCN(C(=O)CCl)C1=C(C)C=CC=C1CC GMDBXHNSCSJZLE-UHFFFAOYSA-N 0.000 claims description 2
- VIKQQGJMQDNWCH-UHFFFAOYSA-N 2-chloro-n-(cyanomethyl)-n-(2,6-dimethylphenyl)acetamide Chemical compound CC1=CC=CC(C)=C1N(CC#N)C(=O)CCl VIKQQGJMQDNWCH-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
- 244000105624 Arachis hypogaea Species 0.000 claims description 2
- WFKSADNZWSKCRZ-UHFFFAOYSA-N Diethatyl-ethyl Chemical compound CCOC(=O)CN(C(=O)CCl)C1=C(CC)C=CC=C1CC WFKSADNZWSKCRZ-UHFFFAOYSA-N 0.000 claims description 2
- 244000020551 Helianthus annuus Species 0.000 claims description 2
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- RZYBVQRHUAFBQE-UHFFFAOYSA-N methyl 2-(n-(2-chloroacetyl)-2,6-dimethylanilino)acetate Chemical compound COC(=O)CN(C(=O)CCl)C1=C(C)C=CC=C1C RZYBVQRHUAFBQE-UHFFFAOYSA-N 0.000 claims description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 2
- MFZYNEGZCZXCSZ-UHFFFAOYSA-N n-but-3-ynyl-2-chloro-n-phenylacetamide Chemical compound C#CCCN(C(=O)CCl)C1=CC=CC=C1 MFZYNEGZCZXCSZ-UHFFFAOYSA-N 0.000 claims description 2
- AEKGSQRXZIDNMI-UHFFFAOYSA-N 2-chloro-n-(cyclohexen-1-yl)-n-propan-2-ylacetamide Chemical compound ClCC(=O)N(C(C)C)C1=CCCCC1 AEKGSQRXZIDNMI-UHFFFAOYSA-N 0.000 claims 2
- HKPHPIREJKHECO-UHFFFAOYSA-N Amichlor Natural products CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims 2
- ZKBAZVCGCOBULN-UHFFFAOYSA-N 2-chloro-n-(1,3-dioxolan-2-ylmethyl)-n-(2-ethyl-6-methylphenyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(=O)CCl)CC1OCCO1 ZKBAZVCGCOBULN-UHFFFAOYSA-N 0.000 claims 1
- IWBVPTHEQYNDFB-UHFFFAOYSA-N 2-chloro-n-(1-methoxypropan-2-yl)-n-(2-methylphenyl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C1=CC=CC=C1C IWBVPTHEQYNDFB-UHFFFAOYSA-N 0.000 claims 1
- UDRNNGBAXFCBLJ-UHFFFAOYSA-N 2-chloro-n-(2,3-dimethylphenyl)-n-propan-2-ylacetamide Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC(C)=C1C UDRNNGBAXFCBLJ-UHFFFAOYSA-N 0.000 claims 1
- WNFVVJKAQZVPBK-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(2-ethoxyethyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC WNFVVJKAQZVPBK-UHFFFAOYSA-N 0.000 claims 1
- QRMXVCIROCSOPW-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(1-methoxybutan-2-yl)acetamide Chemical compound COCC(CC)N(C(=O)CCl)C1=C(C)C=CC=C1C QRMXVCIROCSOPW-UHFFFAOYSA-N 0.000 claims 1
- KJYQOYQOCGXPLR-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C1=C(C)C=CC=C1C KJYQOYQOCGXPLR-UHFFFAOYSA-N 0.000 claims 1
- DWPUVHBGUBPRQS-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(2-methoxypropyl)acetamide Chemical compound COC(C)CN(C(=O)CCl)C1=C(C)C=CC=C1C DWPUVHBGUBPRQS-UHFFFAOYSA-N 0.000 claims 1
- CDACHQNZPZBVKH-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(furan-2-ylmethyl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CC1=CC=CO1 CDACHQNZPZBVKH-UHFFFAOYSA-N 0.000 claims 1
- NAYNDWTXTQPNPI-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(oxolan-2-ylmethyl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CC1OCCC1 NAYNDWTXTQPNPI-UHFFFAOYSA-N 0.000 claims 1
- HJMQOYUROLIRKV-UHFFFAOYSA-N 2-chloro-n-(2-chloro-6-methylphenyl)-n-(2-methoxyethyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1Cl HJMQOYUROLIRKV-UHFFFAOYSA-N 0.000 claims 1
- ZNEWTULDPKTNQN-UHFFFAOYSA-N 2-chloro-n-(2-ethoxyethyl)-n-(2,3,6-trimethylphenyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(C)C=CC(C)=C1C ZNEWTULDPKTNQN-UHFFFAOYSA-N 0.000 claims 1
- CSDFLGOLPKXOBC-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(2-propan-2-yloxyethyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(CCOC(C)C)C(=O)CCl CSDFLGOLPKXOBC-UHFFFAOYSA-N 0.000 claims 1
- GSIADRRHQMXJNC-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-prop-2-ynylacetamide Chemical compound CCC1=CC=CC(C)=C1N(CC#C)C(=O)CCl GSIADRRHQMXJNC-UHFFFAOYSA-N 0.000 claims 1
- ULHCXOHYGYFFPU-UHFFFAOYSA-N 2-chloro-n-(2-methoxyethyl)-n-(2,3,6-trimethylphenyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC(C)=C1C ULHCXOHYGYFFPU-UHFFFAOYSA-N 0.000 claims 1
- NNVRQGZJHLEKBG-UHFFFAOYSA-N 2-chloro-n-(2-methoxyethyl)-n-(2-methoxy-6-methylphenyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1OC NNVRQGZJHLEKBG-UHFFFAOYSA-N 0.000 claims 1
- SXAAVRUIADQETA-UHFFFAOYSA-N 2-chloro-n-(2-methoxyethyl)-n-(2-methylphenyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=CC=CC=C1C SXAAVRUIADQETA-UHFFFAOYSA-N 0.000 claims 1
- 240000006394 Sorghum bicolor Species 0.000 claims 1
- KXAVQXSMZBKSOS-UHFFFAOYSA-N ethyl 2-(n-(2-chloroacetyl)-2,6-dimethylanilino)acetate Chemical compound CCOC(=O)CN(C(=O)CCl)C1=C(C)C=CC=C1C KXAVQXSMZBKSOS-UHFFFAOYSA-N 0.000 claims 1
- WMRNUXKJMBLTLO-UHFFFAOYSA-N n-(2-butoxyethyl)-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC WMRNUXKJMBLTLO-UHFFFAOYSA-N 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract description 4
- 125000003302 alkenyloxy group Chemical group 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 abstract 1
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- 244000061457 Solanum nigrum Species 0.000 description 2
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- 239000013543 active substance Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
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- 150000003863 ammonium salts Chemical class 0.000 description 2
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- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 2
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- ZGSPNIOCEDOHGS-UHFFFAOYSA-L disodium [3-[2,3-di(octadeca-9,12-dienoyloxy)propoxy-oxidophosphoryl]oxy-2-hydroxypropyl] 2,3-di(octadeca-9,12-dienoyloxy)propyl phosphate Chemical compound [Na+].[Na+].CCCCCC=CCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COP([O-])(=O)OCC(O)COP([O-])(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC ZGSPNIOCEDOHGS-UHFFFAOYSA-L 0.000 description 1
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- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Die Erfindung betrifft ein herbizides Mittel enthaltend als Wirkstoff ein Chloracetanilid der Formel I
worin
R¹ und R² unabhängig voneinander Wasserstoff; Halogen; C₁-C₄-Alkyl; C₁-C₄-Alkoxy; C₁-C₄-Halogenalkyl; oder C₁-C₄-Alkoxy-C₁-C₄-alkyl;
Z Wasserstoff; Halogen; oder C₁-C₄-Alkyl;
Y C₁-C₆-Alkylen;
R³ C₁-C₄-Alkoxy; C₃-C₄-Alkenyloxy; Cyano; C₁-C₄-Alkoxycarbonyl; C₁-C₄-Alkyl-CO-NH-; (R⁴)₂N-CO-; Benzoyl; Halogenbenzoyl; einen gegebenenfalls bis zu zweifach gleich oder verschieden durch C₁-C₄-Alkyl substituiertes 1,3-Oxadiazol-2-yl, 1,3-Dioxolan-2-yl, Furan-2-yl, Tetrahydrofuran-2-yl, 1,3,4-Oxadiazol-2-yl, Pyrazol-1-yl, 1,2,4-Triazol-1-yl oder 1,2,4-Triazol-3-yl; (C₁-C₄-Alkoxy)₂CH-; C₁-C₄-Alkyl; Ethinyl; oder 4-Methyl-5-methylthio-1,2,4-triazol-3-yl;
R⁴ unabhängig voneinander je Wasserstoff, C₁-C₄-Alkyl; C₁-C₄-Alkenyl; oder C₁-C₄-Alkinyl bedeutet
neben einer synergistisch wirksamen Menge eines N-Chloracetylcyclohexenamins der Formel II worin
R⁵ C₁-C₆-Alkyl; oder C₃-C₆-Alkenyl; und
R⁶, R⁷, R⁸ und R⁹ unabhängig voneinander Wasserstoff; oder C₁-C₄-Alkyl;
bedeutet.
R¹ und R² unabhängig voneinander Wasserstoff; Halogen; C₁-C₄-Alkyl; C₁-C₄-Alkoxy; C₁-C₄-Halogenalkyl; oder C₁-C₄-Alkoxy-C₁-C₄-alkyl;
Z Wasserstoff; Halogen; oder C₁-C₄-Alkyl;
Y C₁-C₆-Alkylen;
R³ C₁-C₄-Alkoxy; C₃-C₄-Alkenyloxy; Cyano; C₁-C₄-Alkoxycarbonyl; C₁-C₄-Alkyl-CO-NH-; (R⁴)₂N-CO-; Benzoyl; Halogenbenzoyl; einen gegebenenfalls bis zu zweifach gleich oder verschieden durch C₁-C₄-Alkyl substituiertes 1,3-Oxadiazol-2-yl, 1,3-Dioxolan-2-yl, Furan-2-yl, Tetrahydrofuran-2-yl, 1,3,4-Oxadiazol-2-yl, Pyrazol-1-yl, 1,2,4-Triazol-1-yl oder 1,2,4-Triazol-3-yl; (C₁-C₄-Alkoxy)₂CH-; C₁-C₄-Alkyl; Ethinyl; oder 4-Methyl-5-methylthio-1,2,4-triazol-3-yl;
R⁴ unabhängig voneinander je Wasserstoff, C₁-C₄-Alkyl; C₁-C₄-Alkenyl; oder C₁-C₄-Alkinyl bedeutet
neben einer synergistisch wirksamen Menge eines N-Chloracetylcyclohexenamins der Formel II
R⁵ C₁-C₆-Alkyl; oder C₃-C₆-Alkenyl; und
R⁶, R⁷, R⁸ und R⁹ unabhängig voneinander Wasserstoff; oder C₁-C₄-Alkyl;
bedeutet.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH328088 | 1988-09-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP8900138A0 AP8900138A0 (en) | 1989-10-31 |
| AP106A true AP106A (en) | 1990-11-15 |
Family
ID=4252565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1989/000138A AP106A (en) | 1988-09-02 | 1989-08-31 | Synergistic mixture |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP0357557A3 (de) |
| JP (1) | JPH02115102A (de) |
| KR (1) | KR900004254A (de) |
| AP (1) | AP106A (de) |
| AU (1) | AU615571B2 (de) |
| BR (1) | BR8904355A (de) |
| DK (1) | DK434589A (de) |
| FI (1) | FI894074A7 (de) |
| GB (1) | GB2223947A (de) |
| HU (1) | HUT50582A (de) |
| IL (1) | IL91473A0 (de) |
| JO (1) | JO1588B1 (de) |
| MA (1) | MA21622A1 (de) |
| NO (1) | NO893526L (de) |
| NZ (1) | NZ230514A (de) |
| OA (1) | OA09132A (de) |
| PT (1) | PT91595A (de) |
| TN (1) | TNSN89093A1 (de) |
| ZA (1) | ZA896710B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3783988B2 (ja) * | 1997-09-16 | 2006-06-07 | 株式会社ケイディエス | 巻尺 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1618644A1 (de) * | 1966-02-01 | 1971-04-01 | Monsanto Co | Biocide,insbesondere phytotoxische Zubereitungen |
| US3586496A (en) * | 1969-09-15 | 1971-06-22 | Monsanto Co | Herbicidal compositions and use of n-(cycloalken - 1 - yl-) alpha-haloacetamides |
| GB1283163A (en) * | 1970-01-07 | 1972-07-26 | Monsanto Co | Herbicidal compositions |
| FR2479221A1 (fr) * | 1980-03-25 | 1981-10-02 | Monsanto Co | Procede de preparation de 2-haloacetamides a radicaux heterocyclylmethyles, nouveaux produits ainsi obtenus et leur utilisation comme herbicides |
| BE891248A (fr) * | 1980-11-26 | 1982-05-25 | Monsanto Co | Composes de 2-haloacetamides et compositions herbicides contenant ces composes comme ingredients actifs |
| EP0281521A2 (de) * | 1987-03-06 | 1988-09-07 | Ciba-Geigy Ag | Herbizide Zusammensetzungen |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4767396A (en) * | 1987-03-03 | 1988-08-30 | Haemonetics Corporation | Method and apparatus for processing biological fluids |
-
1989
- 1989-05-03 JO JO19891588A patent/JO1588B1/en active
- 1989-08-24 EP EP19890810629 patent/EP0357557A3/de not_active Withdrawn
- 1989-08-29 KR KR1019890012300A patent/KR900004254A/ko not_active Withdrawn
- 1989-08-30 BR BR898904355A patent/BR8904355A/pt unknown
- 1989-08-30 FI FI894074A patent/FI894074A7/fi not_active IP Right Cessation
- 1989-08-30 IL IL91473A patent/IL91473A0/xx unknown
- 1989-08-30 GB GB8919605A patent/GB2223947A/en not_active Withdrawn
- 1989-08-31 PT PT91595A patent/PT91595A/pt unknown
- 1989-08-31 TN TNTNSN89093A patent/TNSN89093A1/fr unknown
- 1989-08-31 AP APAP/P/1989/000138A patent/AP106A/en active
- 1989-08-31 NZ NZ230514A patent/NZ230514A/xx unknown
- 1989-08-31 MA MA21876A patent/MA21622A1/fr unknown
- 1989-09-01 OA OA59637A patent/OA09132A/xx unknown
- 1989-09-01 JP JP1227286A patent/JPH02115102A/ja active Pending
- 1989-09-01 ZA ZA896710A patent/ZA896710B/xx unknown
- 1989-09-01 DK DK434589A patent/DK434589A/da not_active Application Discontinuation
- 1989-09-01 AU AU40993/89A patent/AU615571B2/en not_active Expired - Fee Related
- 1989-09-01 NO NO89893526A patent/NO893526L/no unknown
- 1989-09-01 HU HU894548A patent/HUT50582A/hu unknown
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1618644A1 (de) * | 1966-02-01 | 1971-04-01 | Monsanto Co | Biocide,insbesondere phytotoxische Zubereitungen |
| US3586496A (en) * | 1969-09-15 | 1971-06-22 | Monsanto Co | Herbicidal compositions and use of n-(cycloalken - 1 - yl-) alpha-haloacetamides |
| GB1283163A (en) * | 1970-01-07 | 1972-07-26 | Monsanto Co | Herbicidal compositions |
| FR2479221A1 (fr) * | 1980-03-25 | 1981-10-02 | Monsanto Co | Procede de preparation de 2-haloacetamides a radicaux heterocyclylmethyles, nouveaux produits ainsi obtenus et leur utilisation comme herbicides |
| BE891248A (fr) * | 1980-11-26 | 1982-05-25 | Monsanto Co | Composes de 2-haloacetamides et compositions herbicides contenant ces composes comme ingredients actifs |
| EP0281521A2 (de) * | 1987-03-06 | 1988-09-07 | Ciba-Geigy Ag | Herbizide Zusammensetzungen |
Also Published As
| Publication number | Publication date |
|---|---|
| AP8900138A0 (en) | 1989-10-31 |
| KR900004254A (ko) | 1990-04-12 |
| FI894074A7 (fi) | 1990-03-03 |
| BR8904355A (pt) | 1990-05-08 |
| HUT50582A (en) | 1990-03-28 |
| JPH02115102A (ja) | 1990-04-27 |
| NZ230514A (en) | 1991-01-29 |
| NO893526L (no) | 1990-03-05 |
| ZA896710B (en) | 1990-04-25 |
| DK434589A (da) | 1990-03-03 |
| EP0357557A2 (de) | 1990-03-07 |
| IL91473A0 (en) | 1990-04-29 |
| PT91595A (pt) | 1990-03-30 |
| EP0357557A3 (de) | 1990-09-19 |
| FI894074A0 (fi) | 1989-08-30 |
| GB2223947A (en) | 1990-04-25 |
| OA09132A (fr) | 1991-10-31 |
| AU4099389A (en) | 1990-03-08 |
| GB8919605D0 (en) | 1989-10-11 |
| MA21622A1 (fr) | 1990-04-01 |
| DK434589D0 (da) | 1989-09-01 |
| TNSN89093A1 (fr) | 1991-02-04 |
| NO893526D0 (no) | 1989-09-01 |
| AU615571B2 (en) | 1991-10-03 |
| JO1588B1 (en) | 1989-12-16 |
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