KR920014801A - 치환된 피리딘설폰아미드 화합물 또는 이의 염, 이의 제조방법 및 이를 함유하는 제초제 - Google Patents
치환된 피리딘설폰아미드 화합물 또는 이의 염, 이의 제조방법 및 이를 함유하는 제초제 Download PDFInfo
- Publication number
- KR920014801A KR920014801A KR1019920000898A KR920000898A KR920014801A KR 920014801 A KR920014801 A KR 920014801A KR 1019920000898 A KR1019920000898 A KR 1019920000898A KR 920000898 A KR920000898 A KR 920000898A KR 920014801 A KR920014801 A KR 920014801A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- unsubstituted
- substituted
- amino
- chloro
- 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.)
- Withdrawn
Links
- -1 pyridine sulfonamide compound Chemical class 0.000 title claims abstract 17
- 230000002363 herbicidal effect Effects 0.000 title claims abstract 12
- 150000003839 salts Chemical class 0.000 title claims abstract 9
- 239000004009 herbicide Substances 0.000 title claims abstract 8
- 238000002360 preparation method Methods 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract 15
- 150000001875 compounds Chemical class 0.000 claims abstract 15
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 11
- 125000000547 substituted alkyl group Chemical group 0.000 claims abstract 11
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims abstract 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 10
- 125000005017 substituted alkenyl group Chemical group 0.000 claims abstract 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 19
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 9
- DWJMBQYORXLGAE-UHFFFAOYSA-N pyridine-2-sulfonamide Chemical class NS(=O)(=O)C1=CC=CC=N1 DWJMBQYORXLGAE-UHFFFAOYSA-N 0.000 claims 9
- 239000004480 active ingredient Substances 0.000 claims 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 3
- 239000002671 adjuvant Substances 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000000575 pesticide Substances 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 claims 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 claims 1
- IRCMYGHHKLLGHV-UHFFFAOYSA-N 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl methanesulfonate Chemical compound C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 IRCMYGHHKLLGHV-UHFFFAOYSA-N 0.000 claims 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims 1
- OPQHBTUYQSNUJK-UHFFFAOYSA-N 6-methylsulfanyl-2-n,2-n-di(propan-2-yl)-1,3,5-triazine-2,4-diamine Chemical compound CSC1=NC(N)=NC(N(C(C)C)C(C)C)=N1 OPQHBTUYQSNUJK-UHFFFAOYSA-N 0.000 claims 1
- GXEKYRXVRROBEV-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1CC2C(C(O)=O)C(C(=O)O)C1O2 GXEKYRXVRROBEV-UHFFFAOYSA-N 0.000 claims 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- LRUUNMYPIBZBQH-UHFFFAOYSA-N Methazole Chemical compound O=C1N(C)C(=O)ON1C1=CC=C(Cl)C(Cl)=C1 LRUUNMYPIBZBQH-UHFFFAOYSA-N 0.000 claims 1
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims 1
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 claims 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 1
- JHRPHXGPSIXFSB-UHFFFAOYSA-N [4-(2,4-dichlorophenoxy)phenyl] propaneperoxoate Chemical compound C1=CC(OOC(=O)CC)=CC=C1OC1=CC=C(Cl)C=C1Cl JHRPHXGPSIXFSB-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
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims 1
- WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 claims 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims 1
- 125000004188 dichlorophenyl group Chemical group 0.000 claims 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 1
- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 claims 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
- FFCCBBNQPIMUJI-UHFFFAOYSA-N methyl 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-para-toluate Chemical compound COC(=O)C1=CC=C(C)C=C1C1=NC(C)(C(C)C)C(=O)N1 FFCCBBNQPIMUJI-UHFFFAOYSA-N 0.000 claims 1
- TYIHVCIQMMTVHE-UHFFFAOYSA-N methyl 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-methylbenzoate Chemical compound COC(=O)C1=CC(C)=CC=C1C1=NC(C)(C(C)C)C(=O)N1 TYIHVCIQMMTVHE-UHFFFAOYSA-N 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims 1
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 claims 1
- XOOVLDXDHKQPCR-UHFFFAOYSA-N o-propan-2-yl carbamothioate Chemical compound CC(C)OC(N)=S XOOVLDXDHKQPCR-UHFFFAOYSA-N 0.000 claims 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- RVULBHWZFCBODE-UHFFFAOYSA-M sodium;5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound [Na+].C1=C([N+]([O-])=O)C(C(=O)[O-])=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 RVULBHWZFCBODE-UHFFFAOYSA-M 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical compound S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims 1
- 238000009333 weeding Methods 0.000 claims 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000001228 spectrum Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP91-085718 | 1991-01-24 | ||
| JP8571891 | 1991-01-24 | ||
| JP91-265.553 | 1991-07-12 | ||
| JP26555391 | 1991-07-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR920014801A true KR920014801A (ko) | 1992-08-25 |
Family
ID=26426723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019920000898A Withdrawn KR920014801A (ko) | 1991-01-24 | 1992-01-23 | 치환된 피리딘설폰아미드 화합물 또는 이의 염, 이의 제조방법 및 이를 함유하는 제초제 |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0496608B1 (enExample) |
| JP (1) | JPH0586055A (enExample) |
| KR (1) | KR920014801A (enExample) |
| CN (1) | CN1038012C (enExample) |
| AT (1) | ATE128131T1 (enExample) |
| BR (1) | BR9200189A (enExample) |
| CA (1) | CA2059450A1 (enExample) |
| DE (1) | DE69204859T2 (enExample) |
| ES (1) | ES2078651T3 (enExample) |
| MX (1) | MX9200286A (enExample) |
| RO (1) | RO109448B1 (enExample) |
| RU (1) | RU2054427C1 (enExample) |
| TW (1) | TW201743B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5348933A (en) * | 1991-01-24 | 1994-09-20 | Ishihara Sangyo Kaisha, Ltd. | Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same |
| CA2090807A1 (en) * | 1992-03-10 | 1993-09-11 | Shigeo Murai | Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same |
| DE59309481D1 (de) * | 1992-05-15 | 1999-05-06 | Hoechst Schering Agrevo Gmbh | Synergistisch wirksame Herbizidkombinationen |
| DK0930302T3 (da) * | 1998-01-16 | 2003-07-21 | Hoffmann La Roche | Benzosulfonderivater |
| DE19833007A1 (de) * | 1998-07-23 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Verfahren zur Herstellung von 4,6-disubstituierten 2-Isocyanatopyrimidinen und ihre Verwendung als Zwischenprodukte für Wirkstoffsynthesen |
| BR0015018A (pt) * | 1999-10-26 | 2002-06-18 | Aventis Cropscience Gmbh | Agente herbicida |
| ES2570984T3 (es) | 2003-07-25 | 2016-05-23 | Ishihara Sangyo Kaisha | Composición herbicida que tiene un mayor efecto herbicida y método para aumentar el efecto herbicida |
| KR20240024842A (ko) * | 2021-06-23 | 2024-02-26 | 에프. 호프만-라 로슈 아게 | Nlrp3 억제제의 제조 공정 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US946494A (en) * | 1909-05-15 | 1910-01-11 | George Henry Colebeck | Twine-cutter. |
| EP0116518B1 (de) * | 1983-02-04 | 1987-10-28 | Ciba-Geigy Ag | N-Phenylsulfonyl-N'-pyrimidinyl- und -triazinylharnstoffe |
| US4946494A (en) * | 1987-10-30 | 1990-08-07 | E. I. Du Pont De Nemours And Company | Herbicidal pyridine sulfonylureas |
| AU2809289A (en) * | 1987-11-20 | 1989-06-14 | E.I. Du Pont De Nemours And Company | Herbicidal alkanoylpyridinesulfonylureas |
| DE59007102D1 (de) * | 1989-06-06 | 1994-10-20 | Ciba Geigy Ag | Sulfonylharnstoffe. |
| DE4000503A1 (de) * | 1990-01-10 | 1991-07-11 | Hoechst Ag | Pyridylsulfonylharnstoffe als herbizide und pflanzenwachstumsregulatoren |
| JPH04234850A (ja) * | 1990-02-20 | 1992-08-24 | Ishihara Sangyo Kaisha Ltd | 置換ピリジンスルホンアミド系化合物及びそれらを含有する除草剤 |
-
1992
- 1992-01-16 CA CA002059450A patent/CA2059450A1/en not_active Abandoned
- 1992-01-17 TW TW081100306A patent/TW201743B/zh active
- 1992-01-20 JP JP4046433A patent/JPH0586055A/ja active Pending
- 1992-01-22 RO RO92-200006A patent/RO109448B1/ro unknown
- 1992-01-22 BR BR929200189A patent/BR9200189A/pt not_active Application Discontinuation
- 1992-01-23 EP EP92300564A patent/EP0496608B1/en not_active Expired - Lifetime
- 1992-01-23 DE DE69204859T patent/DE69204859T2/de not_active Expired - Fee Related
- 1992-01-23 MX MX9200286A patent/MX9200286A/es not_active IP Right Cessation
- 1992-01-23 KR KR1019920000898A patent/KR920014801A/ko not_active Withdrawn
- 1992-01-23 ES ES92300564T patent/ES2078651T3/es not_active Expired - Lifetime
- 1992-01-23 RU SU925010744A patent/RU2054427C1/ru active
- 1992-01-23 AT AT92300564T patent/ATE128131T1/de not_active IP Right Cessation
- 1992-01-24 CN CN92101031A patent/CN1038012C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0586055A (ja) | 1993-04-06 |
| TW201743B (enExample) | 1993-03-11 |
| ATE128131T1 (de) | 1995-10-15 |
| CN1064274A (zh) | 1992-09-09 |
| RU2054427C1 (ru) | 1996-02-20 |
| RO109448B1 (ro) | 1995-02-28 |
| EP0496608B1 (en) | 1995-09-20 |
| CA2059450A1 (en) | 1992-07-25 |
| MX9200286A (es) | 1992-10-30 |
| BR9200189A (pt) | 1992-10-06 |
| CN1038012C (zh) | 1998-04-15 |
| EP0496608A1 (en) | 1992-07-29 |
| ES2078651T3 (es) | 1995-12-16 |
| DE69204859T2 (de) | 1996-03-21 |
| DE69204859D1 (de) | 1995-10-26 |
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| Date | Code | Title | Description |
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| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19920123 |
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