JPS6154017B2 - - Google Patents
Info
- Publication number
- JPS6154017B2 JPS6154017B2 JP7021079A JP7021079A JPS6154017B2 JP S6154017 B2 JPS6154017 B2 JP S6154017B2 JP 7021079 A JP7021079 A JP 7021079A JP 7021079 A JP7021079 A JP 7021079A JP S6154017 B2 JPS6154017 B2 JP S6154017B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- present
- weight
- compound
- parts
- 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.)
- Expired
Links
- 230000002363 herbicidal effect Effects 0.000 claims description 17
- 239000004009 herbicide Substances 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- PIZLNJQSSMQFOE-UHFFFAOYSA-N n,2-diphenylpropanamide Chemical compound C=1C=CC=CC=1C(C)C(=O)NC1=CC=CC=C1 PIZLNJQSSMQFOE-UHFFFAOYSA-N 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- AWZJXXWDKOAELM-UHFFFAOYSA-N 2-phenyl-n-[3-(trifluoromethyl)phenyl]acetamide Chemical compound FC(F)(F)C1=CC=CC(NC(=O)CC=2C=CC=CC=2)=C1 AWZJXXWDKOAELM-UHFFFAOYSA-N 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 241000234653 Cyperus Species 0.000 description 5
- 241000209094 Oryza Species 0.000 description 5
- 244000184734 Pyrus japonica Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- -1 m-trifluoromethylphenylacetyl halide Chemical class 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- 241000254158 Lampyridae Species 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 241000218691 Cupressaceae Species 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- FEVJJJQOPGZSIG-UHFFFAOYSA-N 2-[3-(trifluoromethyl)phenyl]acetyl chloride Chemical compound FC(F)(F)C1=CC=CC(CC(Cl)=O)=C1 FEVJJJQOPGZSIG-UHFFFAOYSA-N 0.000 description 1
- MKFHVRPIJCVSLK-UHFFFAOYSA-N 3,3,3-trifluoro-2-phenylpropanamide Chemical compound NC(=O)C(C(F)(F)F)C1=CC=CC=C1 MKFHVRPIJCVSLK-UHFFFAOYSA-N 0.000 description 1
- HQRSIMQXCAWAJB-UHFFFAOYSA-N 3,3,3-trifluoro-2-phenylpropanoic acid Chemical compound OC(=O)C(C(F)(F)F)C1=CC=CC=C1 HQRSIMQXCAWAJB-UHFFFAOYSA-N 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 235000003840 Amygdalus nana Nutrition 0.000 description 1
- 244000296825 Amygdalus nana Species 0.000 description 1
- 240000008853 Datura stramonium Species 0.000 description 1
- 241001076438 Oxya japonica Species 0.000 description 1
- 235000011432 Prunus Nutrition 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 240000000260 Typha latifolia Species 0.000 description 1
- 235000005324 Typha latifolia Nutrition 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- SLUNEGLMXGHOLY-UHFFFAOYSA-N benzene;hexane Chemical compound CCCCCC.C1=CC=CC=C1 SLUNEGLMXGHOLY-UHFFFAOYSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000014774 prunus Nutrition 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011076 safety test Methods 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7021079A JPS55162757A (en) | 1979-06-05 | 1979-06-05 | Meta-trifluoromethylphenylacetanilide and herbicide contaning it as active constituent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7021079A JPS55162757A (en) | 1979-06-05 | 1979-06-05 | Meta-trifluoromethylphenylacetanilide and herbicide contaning it as active constituent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55162757A JPS55162757A (en) | 1980-12-18 |
| JPS6154017B2 true JPS6154017B2 (fr) | 1986-11-20 |
Family
ID=13424924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7021079A Granted JPS55162757A (en) | 1979-06-05 | 1979-06-05 | Meta-trifluoromethylphenylacetanilide and herbicide contaning it as active constituent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS55162757A (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS599521B2 (ja) * | 1981-03-03 | 1984-03-03 | 八洲化学工業株式会社 | 除草剤 |
| JPS60136546A (ja) * | 1983-12-26 | 1985-07-20 | Yashima Chem Ind Co Ltd | 置換フエニル酢酸アニリド誘導体、その製法及び用途 |
| JP4073489B2 (ja) | 1996-05-24 | 2008-04-09 | ニューロサーチ・アクティーゼルスカブ | 酸性基を有するフエニル誘導体、その製造方法及びそれをクロライドチャンネル遮断剤として使用する方法 |
| US6407120B1 (en) | 1999-02-18 | 2002-06-18 | Pfizer Inc. | Neuropeptide Y antagonists |
| EP1033366A3 (fr) * | 1999-02-18 | 2000-12-27 | Pfizer Products Inc. | Dérivés d'amide comme antagonistes de récepteur de Neuropeptide Y (NPY) |
-
1979
- 1979-06-05 JP JP7021079A patent/JPS55162757A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS55162757A (en) | 1980-12-18 |
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