BR0209050B1 - azóis de ação inseticida, processo para produção e uso dos mesmos, bem como agentes para combate de pragas animais e produção dos referidos agentes. - Google Patents
azóis de ação inseticida, processo para produção e uso dos mesmos, bem como agentes para combate de pragas animais e produção dos referidos agentes. Download PDFInfo
- Publication number
- BR0209050B1 BR0209050B1 BRPI0209050-3A BR0209050A BR0209050B1 BR 0209050 B1 BR0209050 B1 BR 0209050B1 BR 0209050 A BR0209050 A BR 0209050A BR 0209050 B1 BR0209050 B1 BR 0209050B1
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- Prior art keywords
- spp
- formula
- methyl
- compounds
- agents
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- 238000000034 method Methods 0.000 title claims description 24
- 241001465754 Metazoa Species 0.000 title claims description 16
- 241000607479 Yersinia pestis Species 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 230000000749 insecticidal effect Effects 0.000 title description 3
- 150000003851 azoles Chemical class 0.000 title description 2
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims description 71
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 27
- 239000003153 chemical reaction reagent Substances 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 19
- 239000000460 chlorine Chemical group 0.000 claims description 18
- 229910052801 chlorine Chemical group 0.000 claims description 17
- 239000003085 diluting agent Substances 0.000 claims description 16
- 229910052731 fluorine Inorganic materials 0.000 claims description 13
- 239000011737 fluorine Substances 0.000 claims description 12
- 125000001153 fluoro group Chemical group F* 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 241000238631 Hexapoda Species 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical group 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 241000239223 Arachnida Species 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000000335 thiazolyl group Chemical group 0.000 claims description 6
- 241000244206 Nematoda Species 0.000 claims description 5
- 238000006396 nitration reaction Methods 0.000 claims description 4
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 4
- 244000078703 ectoparasite Species 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 101000989653 Homo sapiens Membrane frizzled-related protein Proteins 0.000 claims description 2
- 102100029357 Membrane frizzled-related protein Human genes 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- -1 Bicyclic azole derivatives Chemical class 0.000 abstract description 75
- 238000002360 preparation method Methods 0.000 abstract description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 8
- 125000003118 aryl group Chemical group 0.000 abstract description 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 4
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- 241000258242 Siphonaptera Species 0.000 description 6
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- 238000001704 evaporation Methods 0.000 description 6
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- HKSZSGAPTPXYTI-UHFFFAOYSA-N n'-[(6-chloropyridin-3-yl)methyl]ethane-1,2-diamine Chemical compound NCCNCC1=CC=C(Cl)N=C1 HKSZSGAPTPXYTI-UHFFFAOYSA-N 0.000 description 6
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
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- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 4
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- 229960005322 streptomycin Drugs 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 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
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- BUGOPWGPQGYYGR-UHFFFAOYSA-N thiane 1,1-dioxide Chemical compound O=S1(=O)CCCCC1 BUGOPWGPQGYYGR-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- 229940093635 tributyl phosphate Drugs 0.000 description 1
- WVZPYZMQQDNINJ-UHFFFAOYSA-N tributyl(butylstannyloxy)stannane Chemical compound CCCC[SnH](CCCC)O[SnH](CCCC)CCCC WVZPYZMQQDNINJ-UHFFFAOYSA-N 0.000 description 1
- YDUBPEZBWPRJJL-UHFFFAOYSA-M tributyl-(4-chloro-2-phenylphenoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OC1=CC=C(Cl)C=C1C1=CC=CC=C1 YDUBPEZBWPRJJL-UHFFFAOYSA-M 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- 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
- A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
-
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10119422.6 | 2001-04-20 | ||
| DE10119422A DE10119422A1 (de) | 2001-04-20 | 2001-04-20 | Neue insektizid wirkende Azole |
| PCT/EP2002/004176 WO2002085915A2 (de) | 2001-04-20 | 2002-04-16 | Neue insektizid wirkende azole |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR0209050A BR0209050A (pt) | 2004-08-10 |
| BR0209050B1 true BR0209050B1 (pt) | 2012-11-27 |
Family
ID=7682114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0209050-3A BR0209050B1 (pt) | 2001-04-20 | 2002-04-16 | azóis de ação inseticida, processo para produção e uso dos mesmos, bem como agentes para combate de pragas animais e produção dos referidos agentes. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6838462B2 (enExample) |
| EP (1) | EP1383773B1 (enExample) |
| JP (1) | JP4252801B2 (enExample) |
| KR (1) | KR100855915B1 (enExample) |
| CN (1) | CN1289507C (enExample) |
| AT (1) | ATE286059T1 (enExample) |
| AU (1) | AU2002304661B2 (enExample) |
| BR (1) | BR0209050B1 (enExample) |
| CA (1) | CA2444611C (enExample) |
| DE (2) | DE10119422A1 (enExample) |
| ES (1) | ES2232754T3 (enExample) |
| MX (1) | MXPA03009546A (enExample) |
| NO (1) | NO20034662L (enExample) |
| NZ (1) | NZ528961A (enExample) |
| WO (1) | WO2002085915A2 (enExample) |
| ZA (1) | ZA200308087B (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7943160B2 (en) * | 2002-05-09 | 2011-05-17 | Scimetrics Limited Corp. | Pest control methods |
| EP1689231A4 (en) * | 2003-12-04 | 2007-11-14 | Bayer Cropscience Ag | INSECTICIDES N- (HETEROARYL ALKYL) ALKANDIAMINE DERIVATIVES |
| DK1951684T3 (en) * | 2005-11-01 | 2016-10-24 | Targegen Inc | BIARYLMETAPYRIMIDIN kinase inhibitors |
| DE102006015456A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Bicyclische Enamino(thio)carbonylverbindungen |
| RU2379890C1 (ru) * | 2008-11-12 | 2010-01-27 | Общество с ограниченной ответственностью "Анвет" | Бактерицидное средство |
| ES2587954T3 (es) * | 2012-03-29 | 2016-10-27 | Basf Se | Compuestos de hetero-bicíclicos N-sustituidos y derivados para combatir plagas animales II |
| EP2830421B1 (en) | 2012-03-30 | 2017-03-01 | Basf Se | N-substituted pyridinylidene thiocarbonyl compounds and their use for combating animal pests |
| KR20160058863A (ko) | 2013-09-19 | 2016-05-25 | 바스프 에스이 | Ｎ-아실이미노 헤테로시클릭 화합물 |
| WO2017106000A1 (en) | 2015-12-14 | 2017-06-22 | E. I. Du Pont De Nemours And Company | Heterocycle-substituted bicyclic azole pesticides |
| CN114349704A (zh) * | 2022-01-21 | 2022-04-15 | 河南师范大学 | 三氟甲基缀合的吡唑螺环丙烷类化合物及其合成方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3555039A (en) | 1968-01-22 | 1971-01-12 | Sandoz Ag | Imidazo(1,2-c)thiazoles |
| US3578666A (en) | 1968-08-26 | 1971-05-11 | Sandoz Ag | Substituted imidazolines,pyrimidines and diazepines |
| US4098791A (en) | 1977-07-29 | 1978-07-04 | The Upjohn Company | Process for preparing 3-(cyanimino)-3-amino-propionitriles |
| HU180240B (en) | 1978-04-21 | 1983-02-28 | Gyogyszerkutato Intezet | Process for producing new,substituted 1,3-diaryl-2-iminoimidasolidines and 2-imino-hexahydro-pyrimidines |
| US5204360A (en) | 1985-02-04 | 1993-04-20 | Nihon Bayer Agrochem K.K. | Heterocyclic compounds |
| ATE67493T1 (de) | 1985-02-04 | 1991-10-15 | Bayer Agrochem Kk | Heterocyclische verbindungen. |
| US5001138B1 (en) | 1985-02-04 | 1998-01-20 | Bayer Agrochem Kk | Heterocyclic compounds |
| JPH07121909B2 (ja) | 1986-09-10 | 1995-12-25 | 日本バイエルアグロケム株式会社 | 新規複素環式化合物及び殺虫剤 |
| JP2583429B2 (ja) * | 1987-11-06 | 1997-02-19 | 日本バイエルアグロケム株式会社 | イミダゾリン類及び殺虫剤 |
| EP0702670A1 (de) | 1993-06-07 | 1996-03-27 | Bayer Ag | Iodpropargylcarbamate und ihre verwendung als biozide im pflanzen- und materialschutz |
| JPH07126483A (ja) | 1993-11-04 | 1995-05-16 | Polyplastics Co | ポリアセタール樹脂組成物 |
| DE4440837A1 (de) * | 1994-11-15 | 1996-05-23 | Basf Ag | Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper |
-
2001
- 2001-04-16 NZ NZ528961A patent/NZ528961A/en not_active IP Right Cessation
- 2001-04-20 DE DE10119422A patent/DE10119422A1/de not_active Withdrawn
-
2002
- 2002-04-16 EP EP02732621A patent/EP1383773B1/de not_active Expired - Lifetime
- 2002-04-16 CN CNB028116119A patent/CN1289507C/zh not_active Expired - Fee Related
- 2002-04-16 KR KR1020037013208A patent/KR100855915B1/ko not_active Expired - Fee Related
- 2002-04-16 JP JP2002583441A patent/JP4252801B2/ja not_active Expired - Fee Related
- 2002-04-16 BR BRPI0209050-3A patent/BR0209050B1/pt not_active IP Right Cessation
- 2002-04-16 AU AU2002304661A patent/AU2002304661B2/en not_active Ceased
- 2002-04-16 CA CA2444611A patent/CA2444611C/en not_active Expired - Fee Related
- 2002-04-16 ES ES02732621T patent/ES2232754T3/es not_active Expired - Lifetime
- 2002-04-16 US US10/474,934 patent/US6838462B2/en not_active Expired - Fee Related
- 2002-04-16 WO PCT/EP2002/004176 patent/WO2002085915A2/de not_active Ceased
- 2002-04-16 DE DE50201904T patent/DE50201904D1/de not_active Expired - Lifetime
- 2002-04-16 MX MXPA03009546A patent/MXPA03009546A/es active IP Right Grant
- 2002-04-16 AT AT02732621T patent/ATE286059T1/de not_active IP Right Cessation
-
2003
- 2003-10-17 ZA ZA200308087A patent/ZA200308087B/en unknown
- 2003-10-17 NO NO20034662A patent/NO20034662L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20034662D0 (no) | 2003-10-17 |
| ES2232754T3 (es) | 2005-06-01 |
| NO20034662L (no) | 2003-12-10 |
| JP2004527549A (ja) | 2004-09-09 |
| DE10119422A1 (de) | 2002-10-24 |
| US6838462B2 (en) | 2005-01-04 |
| CN1514840A (zh) | 2004-07-21 |
| ATE286059T1 (de) | 2005-01-15 |
| CA2444611C (en) | 2010-07-13 |
| BR0209050A (pt) | 2004-08-10 |
| DE50201904D1 (de) | 2005-02-03 |
| AU2002304661B2 (en) | 2007-04-26 |
| KR20040015091A (ko) | 2004-02-18 |
| EP1383773A2 (de) | 2004-01-28 |
| JP4252801B2 (ja) | 2009-04-08 |
| US20040209896A1 (en) | 2004-10-21 |
| CN1289507C (zh) | 2006-12-13 |
| CA2444611A1 (en) | 2002-10-31 |
| KR100855915B1 (ko) | 2008-09-02 |
| WO2002085915A3 (de) | 2003-01-23 |
| MXPA03009546A (es) | 2004-02-12 |
| EP1383773B1 (de) | 2004-12-29 |
| WO2002085915A2 (de) | 2002-10-31 |
| NZ528961A (en) | 2005-04-29 |
| ZA200308087B (en) | 2004-10-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
| B06A | Patent application procedure suspended [chapter 6.1 patent gazette] | ||
| B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
| B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 27/11/2012, MEDIANTE O RECOLHIMENTO DA TAXA QUINQUENAL DE MANUTENCAO (ARTIGOS 119 E 120 DA LPI) E OBSERVADAS AS DEMAIS CONDICOES LEGAIS. |
|
| B21F | Lapse acc. art. 78, item iv - on non-payment of the annual fees in time | ||
| B24J | Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12) |