DE2333397A1 - Carbothiolate substituierter azepine - Google Patents
Carbothiolate substituierter azepineInfo
- Publication number
- DE2333397A1 DE2333397A1 DE19732333397 DE2333397A DE2333397A1 DE 2333397 A1 DE2333397 A1 DE 2333397A1 DE 19732333397 DE19732333397 DE 19732333397 DE 2333397 A DE2333397 A DE 2333397A DE 2333397 A1 DE2333397 A1 DE 2333397A1
- Authority
- DE
- Germany
- Prior art keywords
- azepine
- spp
- substituted
- dimethyl
- carbothiolate
- 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.)
- Pending
Links
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- -1 oyan Chemical group 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 230000002363 herbicidal effect Effects 0.000 claims description 8
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- 239000004009 herbicide Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
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- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- VDKYRSMVLCBFLS-UHFFFAOYSA-N 2,7-dimethyl-1H-azepine Chemical compound C1=CC=C(NC(=C1)C)C VDKYRSMVLCBFLS-UHFFFAOYSA-N 0.000 claims description 2
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims description 2
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- 241000245665 Taraxacum Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000819233 Tribulus <sea snail> Species 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- 241000249864 Tussilago Species 0.000 description 1
- 241000145124 Uniola Species 0.000 description 1
- 239000005659 Urtica spp. Substances 0.000 description 1
- 240000005592 Veronica officinalis Species 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- 241000405217 Viola <butterfly> Species 0.000 description 1
- 241001106476 Violaceae Species 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 239000001387 apium graveolens Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000009052 artemisia Nutrition 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 150000005130 benzoxazines Chemical group 0.000 description 1
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000001511 capsicum annuum Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- QQSGDKKFXBGYON-UHFFFAOYSA-N ethoxy-methylperoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical class CCOP(=S)(OOC)OC1=CC(C)=NC(C(C)C)=N1 QQSGDKKFXBGYON-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- ZPKLYVJENOZRAW-UHFFFAOYSA-L iron(2+);dichlorate Chemical compound [Fe+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O ZPKLYVJENOZRAW-UHFFFAOYSA-L 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 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 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- YQCIWBXEVYWRCW-UHFFFAOYSA-N methane;sulfane Chemical compound C.S YQCIWBXEVYWRCW-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000001377 petroselinum spp. Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical group 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004892 pyridazines Chemical group 0.000 description 1
- 150000005299 pyridinones Chemical group 0.000 description 1
- 150000003230 pyrimidines Chemical group 0.000 description 1
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 1
- 150000003235 pyrrolidines Chemical class 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 150000003246 quinazolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000006476 reductive cyclization reaction Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical group O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical group 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 150000003585 thioureas Chemical group 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 150000003918 triazines Chemical group 0.000 description 1
- 150000003852 triazoles Chemical group 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732333397 DE2333397A1 (de) | 1973-06-30 | 1973-06-30 | Carbothiolate substituierter azepine |
| IL45023A IL45023A (en) | 1973-06-30 | 1974-06-12 | Carbothiolates and thiocarbothiolates of alkyl-hexahydro-1hazepines their preparation and their use as herbicides |
| JP49068798A JPS5036632A (enrdf_load_html_response) | 1973-06-30 | 1974-06-18 | |
| ZA00744040A ZA744040B (en) | 1973-06-30 | 1974-06-24 | Carbothiolates of substituted azepines |
| BG27082A BG21369A3 (enrdf_load_html_response) | 1973-06-30 | 1974-06-26 | |
| NL7408697A NL7408697A (nl) | 1973-06-30 | 1974-06-27 | Werkwijze voor het bereiden van carbothiolaten van gesubstitueerde azepinen. |
| BR5279/74A BR7405279D0 (pt) | 1973-06-30 | 1974-06-27 | Composicoes a base de carbotiolatos de azepinas substituidas bem como processo para a fabricacao destes compostos |
| OA55233A OA04732A (fr) | 1973-06-30 | 1974-06-27 | Carbothiolates d'azépines substituées. |
| GB2875374A GB1465112A (en) | 1973-06-30 | 1974-06-28 | Carbothiolates of substituted azepines |
| IT51823/74A IT1049293B (it) | 1973-06-30 | 1974-06-28 | Carbotiolati di azepine sostituite |
| ES427821A ES427821A1 (es) | 1973-06-30 | 1974-06-28 | Procedimiento para la obtencion de composiciones herbici- das. |
| DD179577A DD111780A5 (enrdf_load_html_response) | 1973-06-30 | 1974-06-28 | |
| HUBA3098A HU168731B (en) | 1973-06-30 | 1974-06-28 | Herbicides containing substituated aserpin carbotiotates and process for production of the active substances |
| PL1974172259A PL89746B1 (enrdf_load_html_response) | 1973-06-30 | 1974-06-28 | |
| AT536774A AT334681B (de) | 1973-06-30 | 1974-06-28 | Herbizid |
| SE7408583A SE7408583L (enrdf_load_html_response) | 1973-06-30 | 1974-06-28 | |
| BE146007A BE817009A (fr) | 1973-06-30 | 1974-06-28 | Nouveaux carbothiolates de 1h-azepines a activite herbicide selective |
| DK348674A DK348674A (enrdf_load_html_response) | 1973-06-30 | 1974-06-28 | |
| FR7422693A FR2235120B1 (enrdf_load_html_response) | 1973-06-30 | 1974-06-28 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732333397 DE2333397A1 (de) | 1973-06-30 | 1973-06-30 | Carbothiolate substituierter azepine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2333397A1 true DE2333397A1 (de) | 1975-01-23 |
Family
ID=5885606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19732333397 Pending DE2333397A1 (de) | 1973-06-30 | 1973-06-30 | Carbothiolate substituierter azepine |
Country Status (19)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4222765A (en) * | 1976-01-30 | 1980-09-16 | Kumiai Chemical Industry Co., Ltd. | Thiolcarbamic acid esters |
| EP0071683A1 (en) * | 1981-08-04 | 1983-02-16 | Asahi Kasei Kogyo Kabushiki Kaisha | Thiolcarbamate compounds and their use as herbicides |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2632676A1 (de) * | 1976-07-16 | 1978-01-19 | Schering Ag | Trimethylperhydroazepin-1-thiocarbonsaeure-s-aethylester, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes herbizides mittel |
-
1973
- 1973-06-30 DE DE19732333397 patent/DE2333397A1/de active Pending
-
1974
- 1974-06-12 IL IL45023A patent/IL45023A/en unknown
- 1974-06-18 JP JP49068798A patent/JPS5036632A/ja active Pending
- 1974-06-24 ZA ZA00744040A patent/ZA744040B/xx unknown
- 1974-06-26 BG BG27082A patent/BG21369A3/xx unknown
- 1974-06-27 BR BR5279/74A patent/BR7405279D0/pt unknown
- 1974-06-27 OA OA55233A patent/OA04732A/xx unknown
- 1974-06-27 NL NL7408697A patent/NL7408697A/xx unknown
- 1974-06-28 DD DD179577A patent/DD111780A5/xx unknown
- 1974-06-28 ES ES427821A patent/ES427821A1/es not_active Expired
- 1974-06-28 IT IT51823/74A patent/IT1049293B/it active
- 1974-06-28 GB GB2875374A patent/GB1465112A/en not_active Expired
- 1974-06-28 AT AT536774A patent/AT334681B/de not_active IP Right Cessation
- 1974-06-28 PL PL1974172259A patent/PL89746B1/xx unknown
- 1974-06-28 HU HUBA3098A patent/HU168731B/hu unknown
- 1974-06-28 DK DK348674A patent/DK348674A/da unknown
- 1974-06-28 BE BE146007A patent/BE817009A/xx unknown
- 1974-06-28 SE SE7408583A patent/SE7408583L/xx unknown
- 1974-06-28 FR FR7422693A patent/FR2235120B1/fr not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4222765A (en) * | 1976-01-30 | 1980-09-16 | Kumiai Chemical Industry Co., Ltd. | Thiolcarbamic acid esters |
| EP0071683A1 (en) * | 1981-08-04 | 1983-02-16 | Asahi Kasei Kogyo Kabushiki Kaisha | Thiolcarbamate compounds and their use as herbicides |
| US4400199A (en) * | 1981-08-04 | 1983-08-23 | Asahi Kasei Kabashiki Kaisha | Thiolcarbamate compounds and their use as herbicides |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1049293B (it) | 1981-01-20 |
| NL7408697A (nl) | 1975-01-02 |
| FR2235120B1 (enrdf_load_html_response) | 1978-01-13 |
| AT334681B (de) | 1976-01-25 |
| IL45023A0 (en) | 1974-09-10 |
| ZA744040B (en) | 1975-07-30 |
| ES427821A1 (es) | 1976-08-01 |
| FR2235120A1 (enrdf_load_html_response) | 1975-01-24 |
| DK348674A (enrdf_load_html_response) | 1975-02-24 |
| DD111780A5 (enrdf_load_html_response) | 1975-03-12 |
| SE7408583L (enrdf_load_html_response) | 1975-01-02 |
| OA04732A (fr) | 1980-08-31 |
| HU168731B (en) | 1976-07-28 |
| PL89746B1 (enrdf_load_html_response) | 1976-12-31 |
| BE817009A (fr) | 1974-12-30 |
| IL45023A (en) | 1977-10-31 |
| BR7405279D0 (pt) | 1975-01-07 |
| GB1465112A (en) | 1977-02-23 |
| BG21369A3 (enrdf_load_html_response) | 1976-05-20 |
| JPS5036632A (enrdf_load_html_response) | 1975-04-05 |
| ATA536774A (de) | 1976-05-15 |
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