JP2006523553A5 - - Google Patents
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- Publication number
- JP2006523553A5 JP2006523553A5 JP2006505428A JP2006505428A JP2006523553A5 JP 2006523553 A5 JP2006523553 A5 JP 2006523553A5 JP 2006505428 A JP2006505428 A JP 2006505428A JP 2006505428 A JP2006505428 A JP 2006505428A JP 2006523553 A5 JP2006523553 A5 JP 2006523553A5
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- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- optionally
- different
- alkyl
- 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- Withdrawn
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- 150000002367 halogens Chemical class 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- -1 nitro, cyano, thiocyanato, hydroxy Chemical group 0.000 claims description 18
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 16
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 13
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 12
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 12
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 7
- 125000004414 alkyl thio group Chemical group 0.000 claims description 7
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 6
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 6
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 6
- 101100240523 Caenorhabditis elegans nhr-19 gene Proteins 0.000 claims description 5
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 2
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005724 cycloalkenylene group Chemical group 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 229950000688 phenothiazine Drugs 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 229910052802 copper Inorganic materials 0.000 claims 2
- 229910052759 nickel Inorganic materials 0.000 claims 2
- 229910052711 selenium Inorganic materials 0.000 claims 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH3312003 | 2003-03-03 | ||
| PCT/EP2004/050185 WO2004079732A1 (en) | 2003-03-03 | 2004-02-23 | Optical recording materials having high storage density |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006523553A JP2006523553A (ja) | 2006-10-19 |
| JP2006523553A5 true JP2006523553A5 (https=) | 2007-04-19 |
Family
ID=32932301
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006505428A Withdrawn JP2006523553A (ja) | 2003-03-03 | 2004-02-23 | 高度の記録密度を有する光学記録材料類 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20060159882A1 (https=) |
| EP (1) | EP1599878B1 (https=) |
| JP (1) | JP2006523553A (https=) |
| KR (1) | KR20050115265A (https=) |
| CN (1) | CN1757066A (https=) |
| AT (1) | ATE329351T1 (https=) |
| DE (1) | DE602004001135T2 (https=) |
| RU (1) | RU2005130516A (https=) |
| TW (1) | TW200428381A (https=) |
| WO (1) | WO2004079732A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3989846B2 (ja) * | 2001-03-21 | 2007-10-10 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 高い記憶密度を有する光学記録材料 |
| EP1475793B1 (en) * | 2003-04-15 | 2007-12-05 | Ricoh Company, Ltd. | Write-once-read-many optical recording medium and process for recording and reproducing of the optical medium |
| EP1719126A1 (en) * | 2004-02-23 | 2006-11-08 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Optical recording materials having high storage density |
| EP1776423A1 (en) * | 2004-08-10 | 2007-04-25 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Optical recording materials having high storage density |
| EP1710793A1 (de) * | 2005-04-05 | 2006-10-11 | Ciba SC Holding AG | Metallchelate und ihre Verwendung in optischen Aufzeichnungsmedien mit hoher Speicherkapazität |
| KR101745039B1 (ko) * | 2010-01-19 | 2017-06-08 | 스미토모 세이카 가부시키가이샤 | 자외선 흡수 부재용 조성물 및 이것을 이용한 자외선 흡수 부재 |
| JP5400717B2 (ja) * | 2010-06-30 | 2014-01-29 | 住友精化株式会社 | 合成樹脂用安定化剤、該安定化剤を含有する合成樹脂組成物および樹脂部材 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1932894A1 (de) * | 1969-06-28 | 1971-01-28 | Basf Ag | Metallkomplexfarbstoffe |
| DE69725607T2 (de) * | 1996-12-20 | 2004-08-05 | Ciba Speciality Chemicals Holding Inc. | Polymethin-komplex-farbstoffe und ihre verwendung |
| US6162520A (en) * | 1997-09-17 | 2000-12-19 | Mitsui Chemicals, Inc. | Optical recording medium and dipyrromethene metal chelate compound for use therein |
| US6376664B1 (en) * | 1999-03-17 | 2002-04-23 | The Ohio State University | Cyclic bis-benzimidazole ligands and metal complexes thereof |
| US6479123B2 (en) * | 2000-02-28 | 2002-11-12 | Mitsui Chemicals, Inc. | Dipyrromethene-metal chelate compound and optical recording medium using thereof |
| JP3989846B2 (ja) * | 2001-03-21 | 2007-10-10 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 高い記憶密度を有する光学記録材料 |
| EP1719126A1 (en) * | 2004-02-23 | 2006-11-08 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Optical recording materials having high storage density |
-
2004
- 2004-02-23 JP JP2006505428A patent/JP2006523553A/ja not_active Withdrawn
- 2004-02-23 KR KR1020057016423A patent/KR20050115265A/ko not_active Withdrawn
- 2004-02-23 RU RU2005130516/04A patent/RU2005130516A/ru not_active Application Discontinuation
- 2004-02-23 DE DE602004001135T patent/DE602004001135T2/de not_active Expired - Fee Related
- 2004-02-23 EP EP04713552A patent/EP1599878B1/en not_active Expired - Lifetime
- 2004-02-23 AT AT04713552T patent/ATE329351T1/de not_active IP Right Cessation
- 2004-02-23 CN CNA2004800055757A patent/CN1757066A/zh active Pending
- 2004-02-23 WO PCT/EP2004/050185 patent/WO2004079732A1/en not_active Ceased
- 2004-02-23 US US10/546,077 patent/US20060159882A1/en not_active Abandoned
- 2004-03-02 TW TW093105419A patent/TW200428381A/zh unknown
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