SK954482A3 - Tetrahydrophtalimide compounds, manufacturing process threof and herbicidal agent on their base - Google Patents
Tetrahydrophtalimide compounds, manufacturing process threof and herbicidal agent on their base Download PDFInfo
- Publication number
- SK954482A3 SK954482A3 SK9544-82A SK954482A SK954482A3 SK 954482 A3 SK954482 A3 SK 954482A3 SK 954482 A SK954482 A SK 954482A SK 954482 A3 SK954482 A3 SK 954482A3
- Authority
- SK
- Slovakia
- Prior art keywords
- oxygen
- chlorine
- alkyl
- hydrogen
- compounds according
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 46
- 239000004009 herbicide Substances 0.000 title abstract description 12
- 238000004519 manufacturing process Methods 0.000 title description 2
- -1 5-pentyloxy carbonylmethoxy Chemical group 0.000 claims abstract description 45
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 35
- 230000002363 herbicidal effect Effects 0.000 claims description 29
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 15
- 239000000460 chlorine Substances 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- SPAMRUYRVYMHPV-UHFFFAOYSA-N 3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical class C1=CCCC2C(=O)NC(=O)C21 SPAMRUYRVYMHPV-UHFFFAOYSA-N 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000004981 cycloalkylmethyl group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 claims 1
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- CIFFBTOJCKSRJY-UHFFFAOYSA-N 3α,4,7,7α-tetrahydro-1h-isoindole-1,3(2h)-dione Chemical compound C1C=CCC2C(=O)NC(=O)C21 CIFFBTOJCKSRJY-UHFFFAOYSA-N 0.000 abstract description 4
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- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
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- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
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- 125000002091 cationic group Chemical group 0.000 description 1
- 235000003488 common ragweed Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- QHDRKFYEGYYIIK-UHFFFAOYSA-N isovaleronitrile Chemical compound CC(C)CC#N QHDRKFYEGYYIIK-UHFFFAOYSA-N 0.000 description 1
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- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
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- 229920000642 polymer Polymers 0.000 description 1
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- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- 229920005989 resin Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- YALHCTUQSQRCSX-UHFFFAOYSA-N sulfane sulfuric acid Chemical compound S.OS(O)(=O)=O YALHCTUQSQRCSX-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 244000082735 tidal marsh flat sedge Species 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56212396A JPS58110566A (ja) | 1981-12-25 | 1981-12-25 | ２−フエニル−４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
| JP1384582A JPS58131969A (ja) | 1982-01-29 | 1982-01-29 | ２−フェニル−４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
| JP1785882A JPS58135864A (ja) | 1982-02-05 | 1982-02-05 | ２−フェニル−４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
| JP4694082A JPS58162574A (ja) | 1982-03-23 | 1982-03-23 | ２−フエニル−４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
| JP7630682A JPS58192868A (ja) | 1982-05-06 | 1982-05-06 | ２−フェニル−４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル誘導体、その製造法およびそれを有効成分とする除草剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK954482A3 true SK954482A3 (en) | 1997-04-09 |
| SK278417B6 SK278417B6 (en) | 1997-04-09 |
Family
ID=27519566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK9544-82A SK278417B6 (en) | 1981-12-25 | 1982-12-22 | Tetrahydrophtalimide compounds, manufacturing process thereof and herbicidal agent on their base |
Country Status (14)
| Country | Link |
|---|---|
| US (5) | US4670046A (cs) |
| EP (2) | EP0083055B1 (cs) |
| AU (1) | AU557324B2 (cs) |
| BG (2) | BG41995A3 (cs) |
| BR (1) | BR8207478A (cs) |
| CA (1) | CA1181407A (cs) |
| CZ (1) | CZ279697B6 (cs) |
| DE (1) | DE3273387D1 (cs) |
| DK (2) | DK154703C (cs) |
| HU (1) | HU188525B (cs) |
| MY (2) | MY101267A (cs) |
| PL (1) | PL134968B1 (cs) |
| SK (1) | SK278417B6 (cs) |
| UA (1) | UA7085A1 (cs) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU557324B2 (en) * | 1981-12-25 | 1986-12-18 | Sumitomo Chemical Company, Limited | Tetrahydro phthalimide compounds |
| JPS59212472A (ja) * | 1983-05-16 | 1984-12-01 | Sumitomo Chem Co Ltd | ４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル−１，３−ジオン誘導体、その製造法およびそれを有効成分とする除草剤 |
| NL8402253A (nl) * | 1983-07-29 | 1985-02-18 | Sandoz Ag | Nieuwe fenoxyalkylfosfinaten en -fosfonaten. |
| US4902832A (en) * | 1983-08-31 | 1990-02-20 | Sumitomo Chemical Company, Limited | 2-Substituted phenyl-4,5,6,7-tetrahydro-2H-isoindole-1,3-diones, and their production and use |
| JPS6054362A (ja) * | 1983-08-31 | 1985-03-28 | Sumitomo Chem Co Ltd | テトラヒドロフタルイミド誘導体，その製造法およびそれを有効成分とする除草剤 |
| US4563535A (en) * | 1983-09-19 | 1986-01-07 | Sumitomo Chemical Co., Ltd. | Process for producing tetrahydrophthalimides |
| NL8500277A (nl) * | 1984-02-13 | 1985-09-02 | Sandoz Ag | Nieuwe fosfinaten en fosfonaten en werkwijzen voor het bereiden en toepassen van deze verbindingen. |
| HU196892B (en) * | 1984-06-12 | 1989-02-28 | Fmc Corp | Herbicides containing as active substance derivatives of 2-phenil-1,2,4-triasine-3,5-dion and process for production of these derivatives |
| JPH06777B2 (ja) * | 1984-10-03 | 1994-01-05 | 住友化学工業株式会社 | テトラヒドロフタルイミド誘導体およびそれを有効成分とする除草剤 |
| AU574236B2 (en) * | 1984-11-12 | 1988-06-30 | Sumitomo Chemical Company, Limited | Herbicidal composition comprising 2-(4-chloro-2-fluoro-5-n-pentyloxycarbonylmethoxyphenyl) -4,5,6,7-tetrahydro-2h-isoindole-1,3-dione |
| JPH0662373B2 (ja) * | 1984-11-13 | 1994-08-17 | 住友化学工業株式会社 | 除草組成物 |
| DE3603789A1 (de) * | 1986-02-07 | 1987-08-13 | Basf Ag | N-substituierte 3,4,5,6-tetrahydrophthalimide |
| US4917721A (en) * | 1986-02-11 | 1990-04-17 | Ciba-Geigy Corporation | Herbicidal esters, compositions and use |
| USH531H (en) | 1986-06-03 | 1988-10-04 | Anilide herbicide derivatives | |
| IL82657A0 (en) * | 1986-06-03 | 1987-11-30 | Rhone Poulenc Agrochimie | N-(5-substituted methylene)phenyl herbicides |
| ATE67186T1 (de) * | 1986-09-03 | 1991-09-15 | Ciba Geigy Ag | 3-methylphthalimide. |
| US4881967A (en) * | 1986-12-10 | 1989-11-21 | E. I. Du Pont De Nemours And Company | Heterocyclic 2,3-dihydrobenzofuran herbicides |
| US5053071A (en) * | 1986-12-10 | 1991-10-01 | E. I. Du Pont De Nemours And Company | Chromane herbicides |
| US4948418A (en) * | 1986-12-10 | 1990-08-14 | E. I. Du Pont De Nemours And Company | 2,3-dihydrobenzo[b]thiophenes |
| JPH0825970B2 (ja) * | 1987-09-01 | 1996-03-13 | 住友化学工業株式会社 | テトラヒドロフタルイミド系化合物の製造法、その中間体および該中間体の製造法 |
| EP0323271A1 (en) * | 1987-12-30 | 1989-07-05 | Tosoh Corporation | Tetrahydrophthalimide derivative and herbicide composition containing the same |
| US5169428A (en) * | 1987-12-30 | 1992-12-08 | Tosoh Corporation | Tetrahydrophthalimide derivative and herbicide composition containing same |
| DE3835168A1 (de) * | 1988-10-15 | 1990-04-19 | Bayer Ag | N-aryl-stickstoffheterocyclen, mehrere verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| DE3905006A1 (de) * | 1989-02-18 | 1990-08-30 | Bayer Ag | N-aryl-stickstoffheterocyclen mit fluorhaltigen substituenten |
| DE3905916A1 (de) * | 1989-02-25 | 1990-08-30 | Basf Ag | Verwendung von derivaten des n-phenyl-3,4,5,6-tetrahydrophthalimids zur desikkation und abszission von pflanzenorganen |
| USRE37664E1 (en) * | 1989-02-25 | 2002-04-16 | Basf Aktiengessellschaft | Use of derivatives of N-phenl-3,4,5,6-tetrahydrophthalimide for the desiccation and abscission of plant organs |
| WO1993005037A1 (en) * | 1991-09-04 | 1993-03-18 | Ciba-Geigy Ag | Oxetane and thiaetane derivatives |
| TW202380B (cs) * | 1991-10-16 | 1993-03-21 | Sumitomo Chemical Co | |
| JPH0753515A (ja) * | 1993-08-19 | 1995-02-28 | Sumitomo Chem Co Ltd | テトラヒドロフタルイミド誘導体およびそれを有効成分とする除草剤 |
| US5503761A (en) * | 1994-08-02 | 1996-04-02 | Exxon Research & Engineering Co./Hatco Corp. | Technical pentaerythritol esters as lubricant base stock |
| CA2195831A1 (en) * | 1996-01-29 | 1997-07-30 | Bunji Natsume | Phthalimide compound and herbicide containing the same |
| US6528652B1 (en) | 1999-01-21 | 2003-03-04 | Chronimed | Composition and device for detecting leukocytes in urine |
| US6348324B1 (en) | 1999-01-21 | 2002-02-19 | Hypoguard America Limited | Composition and device for detecting leukocytes in urine |
| AU3783100A (en) | 1999-06-14 | 2000-12-21 | Dow Agrosciences Llc | Substituted triazoles, imidazoles and pyrazoles as herbicides |
| JP2002212008A (ja) | 2001-01-22 | 2002-07-31 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| CN100424074C (zh) * | 2005-11-24 | 2008-10-08 | 湖南化工研究院 | 具有除草活性的n-异吲哚二酮取代苯基脲类化合物 |
| CN100465160C (zh) * | 2005-11-24 | 2009-03-04 | 湖南化工研究院 | 具有除草活性的n-异吲哚二酮取代苯基酰胺类化合物 |
| EP2052612A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| DE102008037629A1 (de) * | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| US8759377B2 (en) * | 2009-11-23 | 2014-06-24 | Vanderbilt University | Substituted dioxopiperidines and dioxopyrrolidines as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| CN102286005B (zh) * | 2011-07-01 | 2013-12-25 | 南京工业大学 | 一种合成氟噻乙草酯的方法 |
| WO2014122674A1 (en) | 2013-02-08 | 2014-08-14 | Rallis India Limited | Process for preparation of derivatives of tetrahydrophthalimide |
| CN103283759B (zh) * | 2013-06-26 | 2015-10-28 | 联保作物科技有限公司 | 一种玉米田除草组合物及其制剂 |
| CN105646328B (zh) * | 2014-12-02 | 2018-07-20 | 沈阳中化农药化工研发有限公司 | 一种季铵盐类化合物及其应用 |
| CN119613399A (zh) * | 2023-09-14 | 2025-03-14 | 江西天宇化工有限公司 | 一种含有烷氧乙酸酯取代基的四取代苯甲酸酯类化合物及其应用 |
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| US3808230A (en) * | 1960-01-21 | 1974-04-30 | Delmar Chem | 2-oxy-4-phthaloylamido-5-halobenzoate compounds |
| US3235605A (en) * | 1963-03-01 | 1966-02-15 | Ethyl Corp | Preparation of thiophenylethers |
| US3465001A (en) * | 1966-03-31 | 1969-09-02 | Merck & Co Inc | Maleimido aryloxy alkanoic acids,alkyl esters and amides thereof |
| US3654302A (en) * | 1970-01-30 | 1972-04-04 | Herbert Schwartz | Tetrahydrophthalanils |
| US3984435A (en) * | 1970-12-23 | 1976-10-05 | Mitsubishi Chemical Industries Ltd. | Herbicidal N-substituted-Δ1 -tetrahydrophthalimide |
| US3878224A (en) * | 1970-12-23 | 1975-04-15 | Mitsubishi Chem Ind | N-substituted-{66 {40 -tetrahydrophthalimides |
| DE2223894C3 (de) * | 1972-05-17 | 1981-07-23 | Hoechst Ag, 6000 Frankfurt | Herbizide Mittel auf Basis von Phenoxycarbonsäurederivaten |
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| EP0000351A1 (de) * | 1977-07-07 | 1979-01-24 | Ciba-Geigy Ag | Phenoxy-phenylthio-alkancarbonsäurederivate, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und als Pflanzenwachstumsregulierungsmittel |
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| US4124375A (en) * | 1977-10-12 | 1978-11-07 | Monsanto Company | Substituted phthalimides for regulating the growth of plants |
| FR2433013A1 (fr) * | 1978-08-07 | 1980-03-07 | Rhone Poulenc Agrochimie | Procede de fabrication de l'acide trichloro-2,4,5 phenoxyacetique dont la mise en oeuvre ne necessite pas l'utilisation du trichloro-2,4,5 phenol |
| JPS55130954A (en) * | 1979-03-29 | 1980-10-11 | Sumitomo Chem Co Ltd | Phenylthioacetic acid ester derivative, its preparation, and herbicide containing said compound as effective component |
| US4292070A (en) * | 1979-04-13 | 1981-09-29 | Mitsubishi Chemical Industries, Ltd. | N-Substituted tetrahydrophthalimide and herbicidal composition |
| JPS5724355A (en) * | 1980-07-21 | 1982-02-08 | Mitsui Toatsu Chem Inc | Novel diphenyl ether type compound |
| US4536209A (en) * | 1980-10-07 | 1985-08-20 | Mitsubishi Chemical Industries Ltd. | N-(3-substituted oxyphenyl)tetrahydrophthalimides and herbicidal composition |
| EP0049511A1 (en) * | 1980-10-07 | 1982-04-14 | Mitsubishi Kasei Corporation | Tetrahydrophthalimides and herbicidal composition |
| AU550845B2 (en) * | 1981-03-30 | 1986-04-10 | Sumitomo Chemical Company, Limited | Tetrahydrophthalimides and their starting compounds |
| US4431822A (en) * | 1981-03-30 | 1984-02-14 | Sumitomo Chemical Company, Limited | Tetrahydrophthalimides, and their production and use |
| DE3123157A1 (de) * | 1981-06-11 | 1983-01-05 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von s-aryl-thioglycolsaeuren |
| US4439229A (en) * | 1981-06-29 | 1984-03-27 | Rohm And Haas Company | Substituted phthalimides herbicides |
| US4484941A (en) * | 1981-09-01 | 1984-11-27 | Sumitomo Chemical Company, Limited | Tetrahydrophthalimides, and their production and use as herbicides |
| US4484940A (en) * | 1981-09-01 | 1984-11-27 | Sumitomo Chemical Company, Limited | Tetrahydrophthalimides, and their production and use as herbicides |
| EP0077938A3 (en) * | 1981-10-23 | 1983-08-24 | Mitsubishi Kasei Corporation | N-(3-substituted aminophenyl) tetrahydrophthalimides and herbicidal composition |
| AU557324B2 (en) * | 1981-12-25 | 1986-12-18 | Sumitomo Chemical Company, Limited | Tetrahydro phthalimide compounds |
| EP0095192B1 (en) * | 1982-05-26 | 1988-08-10 | Sumitomo Chemical Company, Limited | Tetrahydrophthalimides, and their production and use |
| JPS59101405A (ja) * | 1982-12-02 | 1984-06-12 | Sumitomo Chem Co Ltd | 除草組成物 |
| JPS59212472A (ja) * | 1983-05-16 | 1984-12-01 | Sumitomo Chem Co Ltd | ４，５，６，７−テトラヒドロ−２ｈ−イソインド−ル−１，３−ジオン誘導体、その製造法およびそれを有効成分とする除草剤 |
| JPS6054362A (ja) * | 1983-08-31 | 1985-03-28 | Sumitomo Chem Co Ltd | テトラヒドロフタルイミド誘導体，その製造法およびそれを有効成分とする除草剤 |
| US4563535A (en) * | 1983-09-19 | 1986-01-07 | Sumitomo Chemical Co., Ltd. | Process for producing tetrahydrophthalimides |
| US4737512A (en) * | 1986-10-27 | 1988-04-12 | Warner-Lambert Company | 4-(substituted-isoindol-2-yl)phenoxy-pentanoic and -heptanoic acids and derivatives as anti-arteriosclerotic agents |
-
1982
- 1982-12-01 AU AU91035/82A patent/AU557324B2/en not_active Ceased
- 1982-12-06 CA CA000417107A patent/CA1181407A/en not_active Expired
- 1982-12-20 EP EP82111841A patent/EP0083055B1/en not_active Expired
- 1982-12-20 EP EP85103131A patent/EP0172306B1/en not_active Expired
- 1982-12-20 DE DE8282111841T patent/DE3273387D1/de not_active Expired
- 1982-12-22 CZ CS829544A patent/CZ279697B6/cs not_active IP Right Cessation
- 1982-12-22 HU HU824131A patent/HU188525B/hu not_active IP Right Cessation
- 1982-12-22 SK SK9544-82A patent/SK278417B6/sk unknown
- 1982-12-23 BR BR8207478A patent/BR8207478A/pt not_active IP Right Cessation
- 1982-12-23 PL PL1982239711A patent/PL134968B1/pl unknown
- 1982-12-23 DK DK573482A patent/DK154703C/da not_active IP Right Cessation
- 1982-12-24 UA UA3525700A patent/UA7085A1/uk unknown
- 1982-12-24 BG BG059040A patent/BG41995A3/xx unknown
-
1983
- 1983-03-09 US US06/473,755 patent/US4670046A/en not_active Expired - Lifetime
-
1986
- 1986-07-21 US US06/887,970 patent/US4770695A/en not_active Expired - Lifetime
- 1986-12-17 US US06/942,703 patent/US4938795A/en not_active Expired - Lifetime
-
1987
- 1987-07-14 MY MYPI87000999A patent/MY101267A/en unknown
- 1987-09-30 US US07/102,617 patent/US4881970A/en not_active Expired - Fee Related
- 1987-09-30 US US07/102,615 patent/US4826533A/en not_active Expired - Fee Related
-
1988
- 1988-05-02 DK DK237988A patent/DK158262C/da not_active IP Right Cessation
- 1988-12-30 MY MY90/88A patent/MY8800090A/xx unknown
-
1994
- 1994-02-24 BG BG098553A patent/BG61119B2/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US4770695A (en) | 1988-09-13 |
| CZ954482A3 (en) | 1995-01-18 |
| US4826533A (en) | 1989-05-02 |
| US4670046A (en) | 1987-06-02 |
| UA7085A1 (uk) | 1995-06-30 |
| DE3273387D1 (en) | 1986-10-23 |
| DK154703C (da) | 1989-06-19 |
| EP0172306B1 (en) | 1988-09-07 |
| CZ279697B6 (cs) | 1995-06-14 |
| DK573482A (da) | 1983-06-26 |
| PL239711A1 (en) | 1984-02-27 |
| EP0083055B1 (en) | 1986-09-17 |
| US4938795A (en) | 1990-07-03 |
| MY101267A (en) | 1991-08-17 |
| CA1181407A (en) | 1985-01-22 |
| EP0172306A1 (en) | 1986-02-26 |
| DK154703B (da) | 1988-12-12 |
| BG61119B2 (bg) | 1996-11-29 |
| BR8207478A (pt) | 1983-10-18 |
| BG41995A3 (en) | 1987-09-15 |
| MY8800090A (en) | 1988-12-31 |
| EP0083055A2 (en) | 1983-07-06 |
| EP0083055A3 (en) | 1983-09-07 |
| DK158262B (da) | 1990-04-23 |
| DK158262C (da) | 1990-10-08 |
| DK237988A (da) | 1988-05-02 |
| US4881970A (en) | 1989-11-21 |
| DK237988D0 (da) | 1988-05-02 |
| PL134968B1 (en) | 1985-09-30 |
| AU9103582A (en) | 1983-06-30 |
| HU188525B (en) | 1986-04-28 |
| SK278417B6 (en) | 1997-04-09 |
| AU557324B2 (en) | 1986-12-18 |
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