CS200510B2 - Herbicide and process for preparing effective compounds - Google Patents
Herbicide and process for preparing effective compounds Download PDFInfo
- Publication number
- CS200510B2 CS200510B2 CS771718A CS171877A CS200510B2 CS 200510 B2 CS200510 B2 CS 200510B2 CS 771718 A CS771718 A CS 771718A CS 171877 A CS171877 A CS 171877A CS 200510 B2 CS200510 B2 CS 200510B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- substituted
- ester
- acid
- salts
- esters
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 7
- 150000001875 compounds Chemical class 0.000 title description 20
- 239000004009 herbicide Substances 0.000 title description 2
- 238000004519 manufacturing process Methods 0.000 title 1
- -1 carbanilic acid ester Chemical class 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 18
- 239000004480 active ingredient Substances 0.000 claims description 7
- AVZJPKADDQKROZ-UHFFFAOYSA-N propan-2-yl n-(3-cyanophenyl)carbamate Chemical group CC(C)OC(=O)NC1=CC=CC(C#N)=C1 AVZJPKADDQKROZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- NJXPYZHXZZCTNI-UHFFFAOYSA-N 3-aminobenzonitrile Chemical compound NC1=CC=CC(C#N)=C1 NJXPYZHXZZCTNI-UHFFFAOYSA-N 0.000 claims description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical class OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 abstract description 3
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 description 19
- 150000002148 esters Chemical class 0.000 description 16
- 150000001408 amides Chemical class 0.000 description 13
- 241000196324 Embryophyta Species 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000007788 liquid Substances 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
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 125000004494 ethyl ester group Chemical group 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
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- 230000000694 effects Effects 0.000 description 2
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- QQZZEFSKUANJGU-UHFFFAOYSA-N ethyl n-(3-cyanophenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(C#N)=C1 QQZZEFSKUANJGU-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
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- PZXBOMMTMFJEBN-UHFFFAOYSA-N (2-chloro-5-cyanophenyl)carbamic acid Chemical compound ClC1=C(NC(O)=O)C=C(C=C1)C#N PZXBOMMTMFJEBN-UHFFFAOYSA-N 0.000 description 1
- UVMTZTPUIFOAGM-UHFFFAOYSA-N (3-chlorophenyl)carbamic acid Chemical compound OC(=O)NC1=CC=CC(Cl)=C1 UVMTZTPUIFOAGM-UHFFFAOYSA-N 0.000 description 1
- LOYXEARIHRYZDG-UHFFFAOYSA-N (3-cyanophenyl)carbamic acid Chemical compound OC(=O)NC1=CC=CC(C#N)=C1 LOYXEARIHRYZDG-UHFFFAOYSA-N 0.000 description 1
- FTDGDIFUDKDKAW-UHFFFAOYSA-N 1,1a,5,5a,6,6a-hexahydrocyclopropa[a]indene Chemical class C12C(CC3CC=CC=C13)C2 FTDGDIFUDKDKAW-UHFFFAOYSA-N 0.000 description 1
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- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- HGBUQKXHEJWLBC-UHFFFAOYSA-N [1,2]thiazolo[4,3-d]pyrimidine 2-oxide Chemical class N1=CN=CC2=NS(=O)C=C21 HGBUQKXHEJWLBC-UHFFFAOYSA-N 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
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- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000008430 aromatic amides Chemical class 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
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 150000005130 benzoxazines Chemical class 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 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
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000002837 defoliant Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 239000003995 emulsifying agent Substances 0.000 description 1
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- 150000001469 hydantoins Chemical class 0.000 description 1
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- 150000002460 imidazoles Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 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
- 150000002576 ketones Chemical class 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
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- 235000019341 magnesium sulphate Nutrition 0.000 description 1
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- NVNYDGHHYOIGAS-UHFFFAOYSA-N methyl n-(3-cyanophenyl)carbamate Chemical compound COC(=O)NC1=CC=CC(C#N)=C1 NVNYDGHHYOIGAS-UHFFFAOYSA-N 0.000 description 1
- NQWMQPKVYVKKDB-UHFFFAOYSA-N methyl n-(5-cyano-2-methylphenyl)carbamate Chemical compound COC(=O)NC1=CC(C#N)=CC=C1C NQWMQPKVYVKKDB-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
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- 235000010446 mineral oil Nutrition 0.000 description 1
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- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- FOFCMCYEVNHTLS-UHFFFAOYSA-N oxazinane-3,4-dione Chemical class O=C1CCONC1=O FOFCMCYEVNHTLS-UHFFFAOYSA-N 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000012071 phase Substances 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
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- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 1
- LJWJBINKEQOKKU-UHFFFAOYSA-N propan-2-yl n-(5-cyano-2-methylphenyl)carbamate Chemical compound CC(C)OC(=O)NC1=CC(C#N)=CC=C1C LJWJBINKEQOKKU-UHFFFAOYSA-N 0.000 description 1
- FLTAYUBQNSRILJ-UHFFFAOYSA-N propyl n-(5-cyano-2-methylphenyl)carbamate Chemical compound CCCOC(=O)NC1=CC(C#N)=CC=C1C FLTAYUBQNSRILJ-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000005299 pyridinones Chemical class 0.000 description 1
- 150000008318 pyrimidones Chemical class 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
- 150000003246 quinazolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
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- 239000000741 silica gel Substances 0.000 description 1
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- 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
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- 150000004867 thiadiazoles Chemical class 0.000 description 1
- OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/32—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C271/38—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762619733 DE2619733A1 (de) | 1976-04-30 | 1976-04-30 | Carbanilsaeureester, verfahren zur herstellung dieser verbindungen sowie diese enthaltende herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS200510B2 true CS200510B2 (en) | 1980-09-15 |
Family
ID=5977066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS771718A CS200510B2 (en) | 1976-04-30 | 1977-03-15 | Herbicide and process for preparing effective compounds |
Country Status (30)
| Country | Link |
|---|---|
| JP (1) | JPS52133946A (xx) |
| AR (1) | AR218245A1 (xx) |
| AT (1) | AT353549B (xx) |
| AU (1) | AU2436577A (xx) |
| BE (1) | BE854128A (xx) |
| BG (1) | BG27715A3 (xx) |
| BR (1) | BR7702183A (xx) |
| CA (1) | CA1100987A (xx) |
| CS (1) | CS200510B2 (xx) |
| DD (1) | DD129732A5 (xx) |
| DE (1) | DE2619733A1 (xx) |
| EG (1) | EG12533A (xx) |
| ES (1) | ES456423A1 (xx) |
| FI (1) | FI771019A (xx) |
| FR (1) | FR2349571A1 (xx) |
| GB (1) | GB1582302A (xx) |
| GR (1) | GR70655B (xx) |
| IE (1) | IE44682B1 (xx) |
| IL (1) | IL51971A0 (xx) |
| IN (1) | IN155907B (xx) |
| IT (1) | IT1075842B (xx) |
| LU (1) | LU77225A1 (xx) |
| NL (1) | NL7701416A (xx) |
| NZ (1) | NZ183795A (xx) |
| PL (1) | PL102202B1 (xx) |
| PT (1) | PT66319B (xx) |
| RO (1) | RO72522A (xx) |
| SE (1) | SE7704519L (xx) |
| SU (2) | SU652861A3 (xx) |
| ZA (1) | ZA772586B (xx) |
-
1976
- 1976-04-30 DE DE19762619733 patent/DE2619733A1/de not_active Withdrawn
-
1977
- 1977-02-10 NL NL7701416A patent/NL7701416A/xx not_active Application Discontinuation
- 1977-03-01 ES ES456423A patent/ES456423A1/es not_active Expired
- 1977-03-01 SU SU772455512A patent/SU652861A3/ru active
- 1977-03-15 CS CS771718A patent/CS200510B2/cs unknown
- 1977-03-17 PT PT66319A patent/PT66319B/pt unknown
- 1977-03-25 AR AR266999A patent/AR218245A1/es active
- 1977-03-30 RO RO7789860A patent/RO72522A/ro unknown
- 1977-04-01 IN IN493/CAL/77A patent/IN155907B/en unknown
- 1977-04-01 FI FI771019A patent/FI771019A/fi not_active Application Discontinuation
- 1977-04-05 NZ NZ183795A patent/NZ183795A/xx unknown
- 1977-04-06 BR BR7702183A patent/BR7702183A/pt unknown
- 1977-04-06 BG BG035930A patent/BG27715A3/xx unknown
- 1977-04-14 CA CA276,170A patent/CA1100987A/en not_active Expired
- 1977-04-18 AU AU24365/77A patent/AU2436577A/en not_active Expired
- 1977-04-20 SE SE7704519A patent/SE7704519L/xx unknown
- 1977-04-25 GB GB17085/77A patent/GB1582302A/en not_active Expired
- 1977-04-25 SU SU772473626A patent/SU655306A3/ru active
- 1977-04-26 EG EG243/77A patent/EG12533A/xx active
- 1977-04-27 IE IE849/77A patent/IE44682B1/en unknown
- 1977-04-28 DD DD7700198641A patent/DD129732A5/xx unknown
- 1977-04-28 JP JP4978177A patent/JPS52133946A/ja active Pending
- 1977-04-28 IT IT22909/77A patent/IT1075842B/it active
- 1977-04-28 LU LU77225A patent/LU77225A1/xx unknown
- 1977-04-28 PL PL1977197702A patent/PL102202B1/pl unknown
- 1977-04-29 ZA ZA00772586A patent/ZA772586B/xx unknown
- 1977-04-29 IL IL51971A patent/IL51971A0/xx unknown
- 1977-04-29 BE BE177153A patent/BE854128A/xx unknown
- 1977-04-29 AT AT305977A patent/AT353549B/de not_active IP Right Cessation
- 1977-04-29 GR GR53331A patent/GR70655B/el unknown
- 1977-05-02 FR FR7713169A patent/FR2349571A1/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| BG27715A3 (en) | 1979-12-12 |
| GB1582302A (en) | 1981-01-07 |
| IE44682L (en) | 1977-10-30 |
| GR70655B (xx) | 1982-12-03 |
| JPS52133946A (en) | 1977-11-09 |
| LU77225A1 (xx) | 1977-08-18 |
| RO72522A (ro) | 1982-09-09 |
| SU652861A3 (ru) | 1979-03-15 |
| PL197702A1 (pl) | 1978-01-02 |
| BE854128A (fr) | 1977-10-31 |
| PL102202B1 (pl) | 1979-03-31 |
| IT1075842B (it) | 1985-04-22 |
| IE44682B1 (en) | 1982-02-24 |
| DE2619733A1 (de) | 1977-11-17 |
| SU655306A3 (ru) | 1979-03-30 |
| FR2349571A1 (fr) | 1977-11-25 |
| AU2436577A (en) | 1978-10-26 |
| ATA305977A (de) | 1979-04-15 |
| CA1100987A (en) | 1981-05-12 |
| DD129732A5 (de) | 1978-02-08 |
| NZ183795A (en) | 1978-11-13 |
| EG12533A (en) | 1979-06-30 |
| SE7704519L (sv) | 1977-10-31 |
| PT66319A (de) | 1977-04-01 |
| BR7702183A (pt) | 1977-12-20 |
| ZA772586B (en) | 1978-03-29 |
| ES456423A1 (es) | 1978-02-01 |
| PT66319B (de) | 1978-08-14 |
| IL51971A0 (en) | 1977-06-30 |
| FI771019A (xx) | 1977-10-31 |
| IN155907B (xx) | 1985-03-23 |
| AR218245A1 (es) | 1980-05-30 |
| AT353549B (de) | 1979-11-26 |
| NL7701416A (nl) | 1977-11-01 |
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