CS201514B2 - Herbicide agent - Google Patents
Herbicide agent Download PDFInfo
- Publication number
- CS201514B2 CS201514B2 CS786026A CS602678A CS201514B2 CS 201514 B2 CS201514 B2 CS 201514B2 CS 786026 A CS786026 A CS 786026A CS 602678 A CS602678 A CS 602678A CS 201514 B2 CS201514 B2 CS 201514B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- compound
- formula
- alkyl
- symbols
- compounds
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- 239000004009 herbicide Substances 0.000 title description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 57
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract 4
- 150000002431 hydrogen Chemical class 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 24
- -1 C6-alkenyl Chemical group 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000004014 thioethyl group Chemical group [H]SC([H])([H])C([H])([H])* 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract description 3
- 229910052717 sulfur Chemical group 0.000 abstract description 3
- 239000011593 sulfur Chemical group 0.000 abstract description 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 239000011521 glass Substances 0.000 description 9
- 239000007921 spray Substances 0.000 description 9
- 239000002689 soil Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000001629 suppression Effects 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- 244000075850 Avena orientalis Species 0.000 description 3
- 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 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003672 ureas Chemical class 0.000 description 3
- HGTXPEOKLIDWIK-UHFFFAOYSA-N 3-chlorocyclohex-2-en-1-one Chemical compound ClC1=CC(=O)CCC1 HGTXPEOKLIDWIK-UHFFFAOYSA-N 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 244000056139 Brassica cretica Species 0.000 description 2
- 235000003351 Brassica cretica Nutrition 0.000 description 2
- 235000003343 Brassica rupestris Nutrition 0.000 description 2
- 241000289659 Erinaceidae Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 235000010460 mustard Nutrition 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000003444 phase transfer catalyst Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 231100000208 phytotoxic Toxicity 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- IBWGNZVCJVLSHB-UHFFFAOYSA-M tetrabutylphosphanium;chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CCCC IBWGNZVCJVLSHB-UHFFFAOYSA-M 0.000 description 2
- SXEZWLWAPDIKRL-UHFFFAOYSA-N 1-(3-hydroxyphenyl)-3-propan-2-ylurea Chemical compound CC(C)NC(=O)NC1=CC=CC(O)=C1 SXEZWLWAPDIKRL-UHFFFAOYSA-N 0.000 description 1
- YAWJSHQHOZHFCI-UHFFFAOYSA-N 1-chloro-5,5-dimethylcyclohexene Chemical compound CC1(C)CCC=C(Cl)C1 YAWJSHQHOZHFCI-UHFFFAOYSA-N 0.000 description 1
- MTFFANYLEXKMTD-UHFFFAOYSA-N 1-hydroxy-1-phenylurea Chemical compound NC(=O)N(O)C1=CC=CC=C1 MTFFANYLEXKMTD-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- DOVGQLDKIZBQJI-UHFFFAOYSA-N 3-chloro-2-methylcyclohex-2-en-1-one Chemical compound CC1=C(Cl)CCCC1=O DOVGQLDKIZBQJI-UHFFFAOYSA-N 0.000 description 1
- YOXBMCKDEYPAQQ-UHFFFAOYSA-N 3-chlorocyclohexan-1-one Chemical compound ClC1CCCC(=O)C1 YOXBMCKDEYPAQQ-UHFFFAOYSA-N 0.000 description 1
- 241000219318 Amaranthus Species 0.000 description 1
- 235000005781 Avena Nutrition 0.000 description 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 235000017896 Digitaria Nutrition 0.000 description 1
- 241001303487 Digitaria <clam> Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 244000088461 Panicum crus-galli Species 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 244000115721 Pennisetum typhoides Species 0.000 description 1
- 235000007195 Pennisetum typhoides Nutrition 0.000 description 1
- 241000295650 Plagiobothrys arizonicus Species 0.000 description 1
- 235000005291 Rumex acetosa Nutrition 0.000 description 1
- 240000007001 Rumex acetosella Species 0.000 description 1
- 235000008515 Setaria glauca Nutrition 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical compound SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical class O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- ZOOSILUVXHVRJE-UHFFFAOYSA-N cyclopropanecarbonyl chloride Chemical compound ClC(=O)C1CC1 ZOOSILUVXHVRJE-UHFFFAOYSA-N 0.000 description 1
- 230000035613 defoliation Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 208000037824 growth disorder Diseases 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000051 modifying effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical class [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 235000003513 sheep sorrel Nutrition 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 125000000446 sulfanediyl group Chemical class *S* 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent 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
- 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<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
-
- 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
- A01N37/22—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 the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—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 the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83409077A | 1977-09-19 | 1977-09-19 | |
| US05/906,495 US4336062A (en) | 1977-09-19 | 1978-05-16 | Herbicidal cyclohexenone derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS201514B2 true CS201514B2 (en) | 1980-11-28 |
Family
ID=27125682
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS786026A CS201514B2 (en) | 1977-09-19 | 1978-09-18 | Herbicide agent |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4336062A (ro) |
| EP (1) | EP0001556B1 (ro) |
| JP (1) | JPS5463050A (ro) |
| AR (1) | AR223152A1 (ro) |
| AU (1) | AU519947B2 (ro) |
| BG (1) | BG30170A3 (ro) |
| BR (1) | BR7806113A (ro) |
| CA (1) | CA1122606A (ro) |
| CS (1) | CS201514B2 (ro) |
| DD (1) | DD141105A5 (ro) |
| DE (1) | DE2860781D1 (ro) |
| DK (1) | DK403578A (ro) |
| ES (1) | ES473475A1 (ro) |
| IL (1) | IL55589A (ro) |
| IT (1) | IT7851103A0 (ro) |
| PH (1) | PH14619A (ro) |
| PL (1) | PL111965B1 (ro) |
| RO (2) | RO80563A (ro) |
| YU (1) | YU222078A (ro) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4762551A (en) * | 1986-06-09 | 1988-08-09 | Stauffer Chemical Company | Certain 3-(substituted thio)-2-benzoyl-cyclohex-2-enones |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA541891A (en) * | 1957-06-04 | D. Stewart William | Polyhalocyclohexenone compositions adapted for herbicidal and other use | |
| DE826133C (de) * | 1948-11-26 | 1951-12-27 | Geigy Ag J R | Verfahren zur Herstellung von Dihydroresorcin-carbaminsaeureestern |
| NL157008B (nl) * | 1966-02-01 | 1978-06-15 | Monsanto Co | Werkwijze voor het bereiden van een preparaat met fytotoxische werking, gevormde preparaten met deze werking, alsmede werkwijze voor het bereiden van n-digesubstitueerde alfa-chlooraceetamidederivaten. |
| US3937726A (en) * | 1966-04-22 | 1976-02-10 | Hoechst Aktiengesellschaft | Urea derivatives and their use as herbicides |
| CH532891A (de) * | 1969-03-26 | 1973-01-31 | Ciba Geigy Ag | Verwendung von Phenylharnstoffen zum selektiven Bekämpfen von Unkräutern in Kulturen von Nutzpflanzen |
| FR2043419A5 (ro) * | 1969-04-28 | 1971-02-12 | Ciba Geigy | |
| US3707365A (en) * | 1970-03-31 | 1972-12-26 | Mobil Oil Corp | Synergistic herbicide combination of cyclohexenone dimers with herbicides |
| US3820975A (en) * | 1970-11-12 | 1974-06-28 | Chemagro Corp | Method for controlling plant growth with substituted cyclohexenones |
| US3781327A (en) * | 1970-12-10 | 1973-12-25 | Stauffer Chemical Co | Meta-carbanilate ethers |
| US3801630A (en) * | 1971-11-11 | 1974-04-02 | American Cyanamid Co | Dioxocyclohexanecarboxanilide insecticides and acaricides |
| DE2411320A1 (de) * | 1974-03-09 | 1975-09-18 | Bayer Ag | (trifluormethylphenoxy)-phenylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| IL48839A0 (en) * | 1975-01-22 | 1976-03-31 | Nippon Soda Co | Novel cyclohexenyloxy-ester derivatives,their preparation and their use as herbicides |
| AU500853B2 (en) * | 1975-07-23 | 1979-06-07 | Stauffer Chemical Company | Diphenyl ether amides |
| US3976470A (en) * | 1975-07-23 | 1976-08-24 | Stauffer Chemical Company | Diphenyl ether amides |
| JPS52111542A (en) * | 1976-03-16 | 1977-09-19 | Sumitomo Chem Co Ltd | Substituted phenylurea derivatives and selective herbicides containing same |
| DE2732811A1 (de) * | 1976-07-23 | 1978-01-26 | Ciba Geigy Ag | Neue cyclopropancarbonsaeurederivate |
| US4149874A (en) * | 1977-06-21 | 1979-04-17 | Stauffer Chemical Company | Substituted cyclopropylmethoxy anilides and their use as herbicides |
| US4230483A (en) * | 1977-06-21 | 1980-10-28 | Stauffer Chemical Company | Substituted cyclopropylmethoxy phenyl carbamates and thiocarbamates and their use as herbicides |
-
1978
- 1978-05-16 US US05/906,495 patent/US4336062A/en not_active Expired - Lifetime
- 1978-09-07 PH PH21583A patent/PH14619A/en unknown
- 1978-09-13 DK DK403578A patent/DK403578A/da not_active Application Discontinuation
- 1978-09-15 CA CA311,367A patent/CA1122606A/en not_active Expired
- 1978-09-15 IT IT7851103A patent/IT7851103A0/it unknown
- 1978-09-16 ES ES473475A patent/ES473475A1/es not_active Expired
- 1978-09-18 DE DE7878100929T patent/DE2860781D1/de not_active Expired
- 1978-09-18 RO RO7895207A patent/RO80563A/ro unknown
- 1978-09-18 AR AR273746A patent/AR223152A1/es active
- 1978-09-18 CS CS786026A patent/CS201514B2/cs unknown
- 1978-09-18 AU AU39933/78A patent/AU519947B2/en not_active Expired
- 1978-09-18 BR BR7806113A patent/BR7806113A/pt unknown
- 1978-09-18 EP EP78100929A patent/EP0001556B1/en not_active Expired
- 1978-09-18 DD DD78207900A patent/DD141105A5/de unknown
- 1978-09-18 BG BG040890A patent/BG30170A3/xx unknown
- 1978-09-18 IL IL55589A patent/IL55589A/xx unknown
- 1978-09-18 RO RO108841A patent/RO84833B/ro unknown
- 1978-09-19 YU YU02220/78A patent/YU222078A/xx unknown
- 1978-09-19 PL PL1978209690A patent/PL111965B1/pl unknown
- 1978-09-19 JP JP11415978A patent/JPS5463050A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU3993378A (en) | 1980-03-27 |
| US4336062A (en) | 1982-06-22 |
| RO84833B (ro) | 1984-09-30 |
| AR223152A1 (es) | 1981-07-31 |
| IT7851103A0 (it) | 1978-09-15 |
| IL55589A0 (en) | 1978-12-17 |
| CA1122606A (en) | 1982-04-27 |
| RO80563A (ro) | 1982-12-06 |
| ES473475A1 (es) | 1979-04-16 |
| EP0001556A3 (en) | 1979-07-11 |
| YU222078A (en) | 1983-04-30 |
| BR7806113A (pt) | 1979-04-17 |
| PL209690A1 (pl) | 1979-06-04 |
| DK403578A (da) | 1979-03-20 |
| DE2860781D1 (en) | 1981-09-24 |
| EP0001556A2 (en) | 1979-05-02 |
| EP0001556B1 (en) | 1981-06-17 |
| RO84833A (ro) | 1984-08-17 |
| JPS5463050A (en) | 1979-05-21 |
| PL111965B1 (en) | 1980-09-30 |
| AU519947B2 (en) | 1982-01-07 |
| PH14619A (en) | 1981-10-12 |
| BG30170A3 (en) | 1981-04-15 |
| DD141105A5 (de) | 1980-04-16 |
| IL55589A (en) | 1981-11-30 |
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