NO771675L - Herbicide midler. - Google Patents
Herbicide midler.Info
- Publication number
- NO771675L NO771675L NO771675A NO771675A NO771675L NO 771675 L NO771675 L NO 771675L NO 771675 A NO771675 A NO 771675A NO 771675 A NO771675 A NO 771675A NO 771675 L NO771675 L NO 771675L
- Authority
- NO
- Norway
- Prior art keywords
- thiadiazoline
- carboxylic acid
- compound according
- chemical compound
- dimethylcarbamoylimino
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 6
- 239000004009 herbicide Substances 0.000 title description 8
- 239000003814 drug Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 33
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- PNWXIVHAFKHCRF-UHFFFAOYSA-N 2-(dimethylcarbamoylimino)-1,3,4-thiadiazole-3-carboxylic acid Chemical class CN(C(=O)N=C1SC=NN1C(=O)O)C PNWXIVHAFKHCRF-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- CPFFMIWOJNRVDE-UHFFFAOYSA-N methyl 2-(dimethylcarbamoylimino)-5-methylsulfanyl-1,3,4-thiadiazole-3-carboxylate Chemical group COC(=O)N1N=C(SC)SC1=NC(=O)N(C)C CPFFMIWOJNRVDE-UHFFFAOYSA-N 0.000 claims description 2
- OVFGZYLIJLMMOS-UHFFFAOYSA-N ethyl 2-(dimethylcarbamoylimino)-5-ethylsulfanyl-1,3,4-thiadiazole-3-carboxylate Chemical group C(C)OC(=O)N1C(SC(=N1)SCC)=NC(N(C)C)=O OVFGZYLIJLMMOS-UHFFFAOYSA-N 0.000 claims 1
- GFVQHFDOPMKUFO-UHFFFAOYSA-N ethyl 2-(dimethylcarbamoylimino)-5-ethylsulfonyl-1,3,4-thiadiazole-3-carboxylate Chemical group CCOC(=O)N1N=C(S(=O)(=O)CC)SC1=NC(=O)N(C)C GFVQHFDOPMKUFO-UHFFFAOYSA-N 0.000 claims 1
- PQHUNICQRBELNW-UHFFFAOYSA-N ethyl 2-(dimethylcarbamoylimino)-5-methylsulfanyl-1,3,4-thiadiazole-3-carboxylate Chemical group CCOC(=O)N1N=C(SC)SC1=NC(=O)N(C)C PQHUNICQRBELNW-UHFFFAOYSA-N 0.000 claims 1
- NRVLKXMRJGTGJC-UHFFFAOYSA-N methyl 2-(dimethylcarbamoylimino)-5-ethylsulfanyl-1,3,4-thiadiazole-3-carboxylate Chemical group CCSC1=NN(C(=O)OC)C(=NC(=O)N(C)C)S1 NRVLKXMRJGTGJC-UHFFFAOYSA-N 0.000 claims 1
- MKIZCXBFBRAUHT-UHFFFAOYSA-N methyl 2-(dimethylcarbamoylimino)-5-ethylsulfonyl-1,3,4-thiadiazole-3-carboxylate Chemical compound CCS(=O)(=O)C1=NN(C(=O)OC)C(=NC(=O)N(C)C)S1 MKIZCXBFBRAUHT-UHFFFAOYSA-N 0.000 claims 1
- HOTXYOPRCDCSOP-UHFFFAOYSA-N methyl 2-(dimethylcarbamoylimino)-5-methylsulfonyl-1,3,4-thiadiazole-3-carboxylate Chemical group COC(=O)N1N=C(S(C)(=O)=O)SC1=NC(=O)N(C)C HOTXYOPRCDCSOP-UHFFFAOYSA-N 0.000 claims 1
- -1 uracils Chemical class 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 17
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 239000013543 active substance Substances 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 150000002736 metal compounds Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
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- 238000002360 preparation method Methods 0.000 description 4
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- 238000003756 stirring Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
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- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
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- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- 241000220261 Sinapis Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000003495 polar organic solvent Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 description 1
- IDAFAPNAZCWRKV-UHFFFAOYSA-N 1,1-dimethyl-3-(1,3,4-thiadiazol-2-yl)urea Chemical class CN(C)C(=O)NC1=NN=CS1 IDAFAPNAZCWRKV-UHFFFAOYSA-N 0.000 description 1
- QUKGLNCXGVWCJX-UHFFFAOYSA-N 1,3,4-thiadiazol-2-amine Chemical class NC1=NN=CS1 QUKGLNCXGVWCJX-UHFFFAOYSA-N 0.000 description 1
- CMQJDYXIZIONAP-UHFFFAOYSA-N 1,3,4-thiadiazol-2-ylurea Chemical class NC(=O)NC1=NN=CS1 CMQJDYXIZIONAP-UHFFFAOYSA-N 0.000 description 1
- 125000000453 2,2,2-trichloroethyl group Chemical group [H]C([H])(*)C(Cl)(Cl)Cl 0.000 description 1
- LPXPCDVHAXMSRH-UHFFFAOYSA-N 2-(dimethylcarbamoylimino)-5-ethylsulfanyl-n,n-dimethyl-1,3,4-thiadiazole-3-carboxamide Chemical compound CCSC1=NN(C(=O)N(C)C)C(=NC(=O)N(C)C)S1 LPXPCDVHAXMSRH-UHFFFAOYSA-N 0.000 description 1
- KIZOOXAPVPXBKD-UHFFFAOYSA-N 2-(dimethylcarbamoylimino)-5-propylsulfonyl-1,3,4-thiadiazole-3-carboxylic acid Chemical compound CN(C(=O)N=C1SC(=NN1C(=O)O)S(=O)(=O)CCC)C KIZOOXAPVPXBKD-UHFFFAOYSA-N 0.000 description 1
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
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- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([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
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 239000004296 sodium metabisulphite Substances 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 229940035339 tri-chlor Drugs 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762621647 DE2621647A1 (de) | 1976-05-13 | 1976-05-13 | 2-(dimethylcarbamoylimino)-1,3,4- thiadiazolin-3-carbonsaeure-ester, verfahren zur herstellung dieser verbindungen sowie diese enthaltende herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO771675L true NO771675L (no) | 1977-11-15 |
Family
ID=5978046
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO771675A NO771675L (no) | 1976-05-13 | 1977-05-12 | Herbicide midler. |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US4169718A (da) |
| JP (1) | JPS52139062A (da) |
| AT (1) | AT354802B (da) |
| AU (1) | AU2513377A (da) |
| BE (1) | BE854614A (da) |
| BG (1) | BG27716A3 (da) |
| CA (1) | CA1090808A (da) |
| CS (1) | CS192480B2 (da) |
| DD (1) | DD130201A5 (da) |
| DE (1) | DE2621647A1 (da) |
| DK (1) | DK114477A (da) |
| ES (1) | ES457730A1 (da) |
| FI (1) | FI771298A (da) |
| FR (1) | FR2351110A1 (da) |
| GB (1) | GB1583271A (da) |
| GR (1) | GR63745B (da) |
| IE (1) | IE45053B1 (da) |
| IL (1) | IL52033A (da) |
| IT (1) | IT1085078B (da) |
| LU (1) | LU76938A1 (da) |
| NL (1) | NL7703889A (da) |
| NO (1) | NO771675L (da) |
| PL (1) | PL102602B1 (da) |
| PT (1) | PT66533B (da) |
| RO (1) | RO72224A (da) |
| SE (1) | SE7705508L (da) |
| SU (2) | SU649320A3 (da) |
| TR (1) | TR19696A (da) |
| ZA (1) | ZA772869B (da) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL293262A (da) * | 1962-05-28 | |||
| DE2124260A1 (de) * | 1971-05-15 | 1972-11-30 | Farbenfabriken Bayer AG, 5090 Le verkusen | Verfahren zur Herstellung von 4 sub stituierten 1,3,4 Thiadiazolon (5) yl (2) harnstoffen |
-
1976
- 1976-05-13 DE DE19762621647 patent/DE2621647A1/de not_active Withdrawn
-
1977
- 1977-03-11 LU LU76938A patent/LU76938A1/xx unknown
- 1977-03-16 DK DK114477A patent/DK114477A/da unknown
- 1977-03-18 CS CS771820A patent/CS192480B2/cs unknown
- 1977-04-07 NL NL7703889A patent/NL7703889A/xx not_active Application Discontinuation
- 1977-04-12 ES ES457730A patent/ES457730A1/es not_active Expired
- 1977-04-12 SU SU772468202A patent/SU649320A3/ru active
- 1977-04-25 FI FI771298A patent/FI771298A/fi not_active Application Discontinuation
- 1977-04-26 BG BG036125A patent/BG27716A3/xx unknown
- 1977-04-28 SU SU772475610A patent/SU648048A3/ru active
- 1977-05-02 GB GB18232/77A patent/GB1583271A/en not_active Expired
- 1977-05-05 IL IL52033A patent/IL52033A/xx unknown
- 1977-05-06 IE IE928/77A patent/IE45053B1/en unknown
- 1977-05-07 RO RO7790253A patent/RO72224A/ro unknown
- 1977-05-10 TR TR19696A patent/TR19696A/xx unknown
- 1977-05-10 US US05/795,642 patent/US4169718A/en not_active Expired - Lifetime
- 1977-05-11 DD DD7700198870A patent/DD130201A5/xx unknown
- 1977-05-11 AT AT336177A patent/AT354802B/de not_active IP Right Cessation
- 1977-05-11 PL PL1977198027A patent/PL102602B1/pl unknown
- 1977-05-11 GR GR53442A patent/GR63745B/el unknown
- 1977-05-11 PT PT66533A patent/PT66533B/pt unknown
- 1977-05-11 SE SE7705508A patent/SE7705508L/xx unknown
- 1977-05-12 IT IT23469/77A patent/IT1085078B/it active
- 1977-05-12 CA CA278,440A patent/CA1090808A/en not_active Expired
- 1977-05-12 NO NO771675A patent/NO771675L/no unknown
- 1977-05-13 JP JP5523377A patent/JPS52139062A/ja active Granted
- 1977-05-13 FR FR7714692A patent/FR2351110A1/fr active Pending
- 1977-05-13 AU AU25133/77A patent/AU2513377A/en not_active Expired
- 1977-05-13 BE BE177559A patent/BE854614A/xx unknown
- 1977-05-13 ZA ZA00772869A patent/ZA772869B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1090808A (en) | 1980-12-02 |
| CS192480B2 (en) | 1979-08-31 |
| PT66533B (de) | 1978-10-17 |
| BG27716A3 (en) | 1979-12-12 |
| JPS5538342B2 (da) | 1980-10-03 |
| IL52033A0 (en) | 1977-07-31 |
| SU649320A3 (ru) | 1979-02-25 |
| DE2621647A1 (de) | 1977-12-01 |
| JPS52139062A (en) | 1977-11-19 |
| FR2351110A1 (fr) | 1977-12-09 |
| PL102602B1 (pl) | 1979-04-30 |
| ATA336177A (de) | 1979-06-15 |
| PT66533A (de) | 1977-06-01 |
| FI771298A (da) | 1977-11-14 |
| TR19696A (tr) | 1979-10-11 |
| DD130201A5 (de) | 1978-03-15 |
| PL198027A1 (pl) | 1978-02-13 |
| DK114477A (da) | 1977-11-14 |
| US4169718A (en) | 1979-10-02 |
| IL52033A (en) | 1980-03-31 |
| ZA772869B (en) | 1978-03-29 |
| IE45053B1 (en) | 1982-06-16 |
| ES457730A1 (es) | 1978-02-16 |
| BE854614A (fr) | 1977-11-14 |
| IT1085078B (it) | 1985-05-28 |
| SU648048A3 (ru) | 1979-02-15 |
| LU76938A1 (da) | 1977-07-14 |
| GB1583271A (en) | 1981-01-21 |
| IE45053L (en) | 1977-11-13 |
| GR63745B (en) | 1979-12-04 |
| AU2513377A (en) | 1978-11-16 |
| NL7703889A (nl) | 1977-11-15 |
| RO72224A (ro) | 1982-05-10 |
| SE7705508L (sv) | 1977-11-14 |
| AT354802B (de) | 1979-01-25 |
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