KR840003005A - 3,5-비스(트리플루오로메틸)페녹시 카르복실산과 그 유도체 - Google Patents
3,5-비스(트리플루오로메틸)페녹시 카르복실산과 그 유도체 Download PDFInfo
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- KR840003005A KR840003005A KR1019830000356A KR830000356A KR840003005A KR 840003005 A KR840003005 A KR 840003005A KR 1019830000356 A KR1019830000356 A KR 1019830000356A KR 830000356 A KR830000356 A KR 830000356A KR 840003005 A KR840003005 A KR 840003005A
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- Prior art keywords
- trifluoromethyl
- bis
- phenoxy
- group
- emollient
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- PBBCJJKBBKHEQE-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenyl] hydrogen carbonate Chemical compound OC(=O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 PBBCJJKBBKHEQE-UHFFFAOYSA-N 0.000 title 1
- 239000003974 emollient agent Substances 0.000 claims 13
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims 10
- 239000004009 herbicide Substances 0.000 claims 10
- 230000002363 herbicidal effect Effects 0.000 claims 9
- 238000000034 method Methods 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 239000008141 laxative Substances 0.000 claims 7
- 230000002475 laxative effect Effects 0.000 claims 7
- 239000012429 reaction media Substances 0.000 claims 7
- 229960001413 acetanilide Drugs 0.000 claims 5
- 239000007921 spray Substances 0.000 claims 5
- -1 3,5-bis (trifluoromethyl) phenoxy compound Chemical class 0.000 claims 4
- ODSXJQYJADZFJX-UHFFFAOYSA-N 3,5-bis(trifluoromethyl)phenol Chemical compound OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 ODSXJQYJADZFJX-UHFFFAOYSA-N 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 239000002689 soil Substances 0.000 claims 4
- 239000003960 organic solvent Substances 0.000 claims 3
- LAICZTCYXNZHMU-UHFFFAOYSA-N 2-[3,5-bis(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 LAICZTCYXNZHMU-UHFFFAOYSA-N 0.000 claims 2
- 240000000111 Saccharum officinarum Species 0.000 claims 2
- 235000007201 Saccharum officinarum Nutrition 0.000 claims 2
- 238000005507 spraying Methods 0.000 claims 2
- RZNJETZNBTYBEE-UHFFFAOYSA-N 2-[3,5-bis(trifluoromethyl)phenoxy]-n-methylacetamide Chemical compound CNC(=O)COC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 RZNJETZNBTYBEE-UHFFFAOYSA-N 0.000 claims 1
- MKKVSRBOJJBGDN-UHFFFAOYSA-N 2-[3,5-bis(trifluoromethyl)phenoxy]acetamide Chemical compound NC(=O)COC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 MKKVSRBOJJBGDN-UHFFFAOYSA-N 0.000 claims 1
- ZPRVUSMSDMDKLC-UHFFFAOYSA-N 2-[3,5-bis(trifluoromethyl)phenoxy]propanamide Chemical compound NC(=O)C(C)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 ZPRVUSMSDMDKLC-UHFFFAOYSA-N 0.000 claims 1
- LDBQWACSYCEHTM-UHFFFAOYSA-N 2-[3,5-bis(trifluoromethyl)phenoxy]propanoic acid Chemical compound OC(=O)C(C)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 LDBQWACSYCEHTM-UHFFFAOYSA-N 0.000 claims 1
- PYCDGFWHAUMZRO-UHFFFAOYSA-N 2-chloro-n-(2-methoxy-6-methylphenyl)-n-propan-2-ylacetamide Chemical compound COC1=CC=CC(C)=C1N(C(C)C)C(=O)CCl PYCDGFWHAUMZRO-UHFFFAOYSA-N 0.000 claims 1
- YFULBSABQLIMLH-UHFFFAOYSA-N 4-[3,5-bis(trifluoromethyl)phenoxy]butanoic acid Chemical compound OC(=O)CCCOC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 YFULBSABQLIMLH-UHFFFAOYSA-N 0.000 claims 1
- AQDRWJSTORCZMK-UHFFFAOYSA-N O-[3,5-bis(trifluoromethyl)phenyl]hydroxylamine Chemical compound NOC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 AQDRWJSTORCZMK-UHFFFAOYSA-N 0.000 claims 1
- MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 claims 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- AOCYNFHGXQOVRY-UHFFFAOYSA-N ethyl 2-[3,5-bis(trifluoromethyl)phenoxy]acetate Chemical compound CCOC(=O)COC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 AOCYNFHGXQOVRY-UHFFFAOYSA-N 0.000 claims 1
- XKTOWUXTSFHYKE-UHFFFAOYSA-N ethyl 2-[3,5-bis(trifluoromethyl)phenoxy]propanoate Chemical compound CCOC(=O)C(C)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 XKTOWUXTSFHYKE-UHFFFAOYSA-N 0.000 claims 1
- CZLJFYOZGUYSFW-UHFFFAOYSA-N ethyl 4-[3,5-bis(trifluoromethyl)phenoxy]butanoate Chemical compound CCOC(=O)CCCOC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 CZLJFYOZGUYSFW-UHFFFAOYSA-N 0.000 claims 1
- 230000009931 harmful effect Effects 0.000 claims 1
- AMLQVJSODCJJPX-UHFFFAOYSA-N methyl 2-[3,5-bis(trifluoromethyl)phenoxy]acetate Chemical compound COC(=O)COC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 AMLQVJSODCJJPX-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 159000000000 sodium salts Chemical class 0.000 claims 1
- 238000009331 sowing Methods 0.000 claims 1
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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- 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
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
- C07C59/70—Ethers of hydroxy-acetic acid, e.g. substitutes on the ring
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- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (31)
- 적어도 1종의 아세트 아닐라이드 제초제를 다음과 같은 구조식을 갖는 완화제유효량과 함께 농작물부위에 뿌림으로서 제초제의 유해효과를 감소시키는 완화제의 이용방법.여기서 R1은 수소나 C1-C5알킬로 구성된 기로부터 독립적으로 선택되며 n은 1-5의 정수, R2는 다음과 같은 것들은 구성된기로 부터 선택된다.여기서 R3는 C1-C5알킬, 농업적으로 적합한 양이온으로 구성된 기로부터 선택되며, R4는 수소나 C1-C5알킬로 구성된 기로부터 독립적으로 선택된다.
- 제1항에 있어서 완화제의 이용방법은 완화제를 농작물의 종자에 사전 피복한후 토양에 파종하고 제초제를 뿌리는 것.
- 제1항에 있어서 완화제의 이용방법은 제초제를 종자나 파종된 토양에 뿌리고 완화제를 뿌리는 것.
- 제1항에 있어서 완화제의 이용방법은 완화제를 종자가 파종된 토양에 뿌리고 제초제를 뿌리는 것.
- 제1항에 있어서 완화제의 이용방법은 완화제와 제초제를 혼합한 혼합물은 종자가 파종된 토양에 뿌리는 것.
- 제2,3,4,5항에 있어서 완화제는 4-[3,5-비스(트리플루오로메틸)페녹시]부타노익에시드.
- 제2,3,4,5항에 있어서 완화제는 에틸 4-[3,5-비스(트리플루오로메틸)페녹시]부티레이트.
- 제2,3,4,5항에 있어서 완화제는 2-[3,5-비스(트리플루오로메틸)페녹시]프로피오닉에시드.
- 제2,3,4,5항에 있어서 완화제는 [3,5-비스(트리플루오로메틸)페녹시]아세틱에시드.
- 제2,3,4,5항에 있어서 완화제는 메틸 [3,5-비스(트리플루오로메틸)페녹시]아세테이트.
- 제2,3,4,5항에 있어서 완화제는 2-[3,5-비스(트리플루오로메틸)페녹시]프로판아미드.
- 제2,3,4,5항에 있어서 완화제는 에틸 [3,5-비스(트리플루오로메틸)페녹시]아세테이트.
- 제2,3,4,5항에 있어서 완화제는 N-메틸 2-[3,5-비스(트리플루오로메틸)페녹시]아세트아미드.
- 제2,3,4,5항에 있어서 완화제는 2-[3,5-비스(트리플루오로메틸)페녹시]아세트아미드.
- 제2,3,4,5항에 있어서 완화제는 [3,5-비스(트리플루오로메틸)페녹시]아세틱에시드의 나트륨염.
- 제2,3,4,5항에 있어서 완화제는 에틸 2-[3,5-비스(트리플루오로메틸)페녹시]프로피오네이트.
- 제2,3,4,5항에 있어서 아세트 아닐라이드 제초제는 2-클로로-2′, 6′-디에틸-N-(메톡시메틸)아세트 아닐라이드.
- 제2,3,4,5항에 있어서 아세트 아닐라이드 제초제는 2-클로로-2′, 6′-디에틸-N-(부톡시메틸)아세트 아닐라이드.
- 제2,3,4,5항에 있어서 아세트 아닐라이드 제초제는 2,3,3-트리클로로알릴 디이소프로필티오 카바메이트.
- 제2,3,4,5항에 있어서 아세트 아닐라이드 제초제는 2-클로로-2′-메틸- 6′-메톡시-N-(이소프로필)아세트 아닐라이드.
- 제1항에 있어서 농작물의 종류는 사탕수수이다.
- 제2,3,4,5항에 있어서 농작물의 종류는 사탕수수이다.
- 염기성 조건하에서 3,5-디트리플루오로 메틸페놀과 다음 일반식을 가지는 화합물을 반응시켜 3,5-비스(트리플루오로메틸)페녹시 화합물을 제조하는 방법.R - X여기에서 R은 다음 구조식을 갖는다.여기에서 R1수소와 C1-C5알킬로 구성된 기로부터 독립선택되고 n은 1-5의 정수, R2는 로 구성된 기로부터 독립선택되며 여기서 X는 할로겐이며 반응매질로부터 페녹시 화합물을 분리한다.
- 염기성 반응 매질존재하에서 3,5-디트리플루오로메틸페놀과 다음 일반식을 가지는 화합물을 반응시켜 3,5-비스(트리플루오로메틸)페녹시 화합물을 제조하는 방법.R - X여기서 R은 다음과 같은 구조식을 갖는다.여기서 R1은 수소와 C1-C5알킬로 구성된 기로부터 독립선택되고 n은 1-5의 정수, R2는 로 구성된 기로부터 선택된다. 여기에서 R3는 C1C5알킬, R4는 수소와 C1-C5알킬로 구성된기로부터 선택되며 X는 할로겐, 이반응은 0-100℃의온도에서 반응시킨다.
- 제24항에 있어서 반응매질은 불활성유기용매이다.
- 제24항에 있어서 반응매질은 염기성수용액이다.
- 제25항에 있어서 반응온도는 환류온도이다.
- 염기성 반응매질 존재하에서 3,5-디트리플루오로메틸페놀과 다음의 일반식을 가지는 화합물을 반응시켜 3,5-비스(트리플루오로메틸)페녹시 아미드를 제조하는 방법.여기에서 R1과 R4는 수소나 C1-C5알킬로 구성된 기로부터 독립적으로 선택되며 X는 할로겐이다.
- 제28항에 있어서 반응매질은 불활성 유기용매이며 반응온도는 0-100℃이다.
- 염기성 매질 존재하에서 3,5-디트리플루오로메틸페놀과 다음의 구조식을 가지는 화합물을 반응시켜 3,5-비스(트리플루오로메틸)페녹시 에스테르를 제조하는 방법.여기에서 R1과 R3는 수소와 C1-C5알킬로 구성된기로 부터 독립적으로 선택되며 X는 할로겐이다.
- 제30항에 있어서 반응매질은 불활성유기용매이고 반응온도는 0-100℃이다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/344,652 US4416687A (en) | 1982-02-01 | 1982-02-01 | 3,5-Bis (trifluoromethyl)phenoxy carboxylic acids and derivatives thereof |
| US344652 | 1982-02-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR840003005A true KR840003005A (ko) | 1984-08-13 |
| KR850001330B1 KR850001330B1 (ko) | 1985-09-19 |
Family
ID=23351409
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019830000356A KR850001330B1 (ko) | 1982-02-01 | 1983-01-31 | 3, 5-비스(트리플루오로메틸)페녹시 카르복실산과 그 유도체 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4416687A (ko) |
| EP (1) | EP0088066B1 (ko) |
| JP (1) | JPS58134048A (ko) |
| KR (1) | KR850001330B1 (ko) |
| AU (1) | AU554260B2 (ko) |
| BR (1) | BR8300476A (ko) |
| DE (1) | DE3360085D1 (ko) |
| ES (1) | ES519346A0 (ko) |
| NO (1) | NO155132C (ko) |
| NZ (1) | NZ203138A (ko) |
| PH (1) | PH18317A (ko) |
| PT (1) | PT76173B (ko) |
| ZA (1) | ZA83617B (ko) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3404401C2 (de) * | 1984-02-08 | 1994-02-10 | Hoechst Ag | Verwendung von Aryloxy-Verbindungen als Antidots |
| US4859234A (en) * | 1987-09-14 | 1989-08-22 | Ici Americas Inc. | Herbicidal compositions of acylated 1,3-dicarbonyl herbicides and phenoxyalkanoic acids, salts, amides and esters therof as antidotes |
| DE4217928A1 (de) * | 1992-05-30 | 1993-12-02 | Hoechst Ag | Neue Mischungen aus Herbiziden und Antidots, neue (Hetero-)Aryloxy-Verbindungen, Verfahren zu deren Herstellung, diese enthaltenden Mittel und deren Verwendung |
| FR2698873B1 (fr) * | 1992-12-07 | 1995-02-24 | Lipha | Benzocycloheptènes, benzoxépines et benzothiépines activateurs des canaux potassiques, procédé de préparation, composition pharmaceutique les contenant. |
| TW259690B (ko) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| EP1917864A1 (en) | 2006-11-01 | 2008-05-07 | Nestec S.A. | Soluble foaming beverage powder |
| EP3368509A4 (en) * | 2015-10-30 | 2019-05-01 | Trillium Therapeutics Inc. | FLUORINATED AMIDE DERIVATIVES AND THEIR USES AS THERAPEUTIC AGENTS |
| US11512067B2 (en) | 2017-09-14 | 2022-11-29 | Daiichi Sankyo Company, Limited | Compound having cyclic structure |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR6679625D0 (pt) * | 1965-05-27 | 1973-10-23 | Merck & Co Inc | Processo para preparar acidos carboxilicos |
| US3617245A (en) * | 1966-04-07 | 1971-11-02 | Fujisawa Pharmaceutical Co | Compositions and methods for controlling plant growth |
| BE795943A (fr) * | 1972-02-29 | 1973-08-27 | Bayer Ag | Nouveaux derives de 2,4-bis (trifluoromethyl)2-6-nitrophenol, leur procede de preparation et leur application comme herbicides |
| GB2024213B (en) * | 1978-06-30 | 1982-09-08 | Ici Ltd | Dihalophenoxypropionic acids and their derivatives and their use as cotton desiccants |
-
1982
- 1982-02-01 US US06/344,652 patent/US4416687A/en not_active Expired - Fee Related
-
1983
- 1983-01-28 DE DE8383870005T patent/DE3360085D1/de not_active Expired
- 1983-01-28 ES ES519346A patent/ES519346A0/es active Granted
- 1983-01-28 AU AU10848/83A patent/AU554260B2/en not_active Expired - Fee Related
- 1983-01-28 EP EP83870005A patent/EP0088066B1/en not_active Expired
- 1983-01-31 NZ NZ203138A patent/NZ203138A/en unknown
- 1983-01-31 NO NO830320A patent/NO155132C/no unknown
- 1983-01-31 ZA ZA83617A patent/ZA83617B/xx unknown
- 1983-01-31 PT PT76173A patent/PT76173B/pt unknown
- 1983-01-31 PH PH28457A patent/PH18317A/en unknown
- 1983-01-31 BR BR8300476A patent/BR8300476A/pt unknown
- 1983-01-31 KR KR1019830000356A patent/KR850001330B1/ko active IP Right Grant
- 1983-01-31 JP JP58013022A patent/JPS58134048A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BR8300476A (pt) | 1983-11-01 |
| EP0088066B1 (en) | 1985-04-03 |
| AU1084883A (en) | 1983-08-11 |
| NO155132C (no) | 1987-02-18 |
| ZA83617B (en) | 1983-12-28 |
| ES8403093A1 (es) | 1984-03-01 |
| PT76173A (en) | 1983-02-01 |
| KR850001330B1 (ko) | 1985-09-19 |
| NO830320L (no) | 1983-08-02 |
| ES519346A0 (es) | 1984-03-01 |
| PH18317A (en) | 1985-05-29 |
| DE3360085D1 (en) | 1985-05-09 |
| US4416687A (en) | 1983-11-22 |
| JPS58134048A (ja) | 1983-08-10 |
| NO155132B (no) | 1986-11-10 |
| PT76173B (en) | 1985-11-11 |
| NZ203138A (en) | 1986-03-14 |
| AU554260B2 (en) | 1986-08-14 |
| EP0088066A1 (en) | 1983-09-07 |
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| Date | Code | Title | Description |
|---|---|---|---|
| E701 | Decision to grant or registration of patent right |