JP6098158B2 - 化合物 - Google Patents
化合物 Download PDFInfo
- Publication number
- JP6098158B2 JP6098158B2 JP2012282208A JP2012282208A JP6098158B2 JP 6098158 B2 JP6098158 B2 JP 6098158B2 JP 2012282208 A JP2012282208 A JP 2012282208A JP 2012282208 A JP2012282208 A JP 2012282208A JP 6098158 B2 JP6098158 B2 JP 6098158B2
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- JP
- Japan
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- 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.)
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- 0 CC(C1C*CC1)=C(C)c(cc1*(c2ccc(*)cc2)=O)c(C)cc1N Chemical compound CC(C1C*CC1)=C(C)c(cc1*(c2ccc(*)cc2)=O)c(C)cc1N 0.000 description 5
- NSELYKZLLNWRED-UHFFFAOYSA-N C=C1CCOCC1 Chemical compound C=C1CCOCC1 NSELYKZLLNWRED-UHFFFAOYSA-N 0.000 description 1
- WHFHZEJSZFHFCS-UHFFFAOYSA-N C=CC(OCC(C1)C2C(CC3OC33)C3C1C2)=O Chemical compound C=CC(OCC(C1)C2C(CC3OC33)C3C1C2)=O WHFHZEJSZFHFCS-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N C=Cc1ccccc1 Chemical compound C=Cc1ccccc1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- QGBSDNCTLUIBSW-UHFFFAOYSA-N CC(C)(CC(C)(C)C1)CC1(c1ccc2[o]c(C)nc2c1)c1cc(N=C(C)C2OC22)c2cc1 Chemical compound CC(C)(CC(C)(C)C1)CC1(c1ccc2[o]c(C)nc2c1)c1cc(N=C(C)C2OC22)c2cc1 QGBSDNCTLUIBSW-UHFFFAOYSA-N 0.000 description 1
- CBCICFOJVZPSPH-UHFFFAOYSA-N CC(C)(c1cc(Br)c2[o]c(C)nc2c1)c(cc1Br)cc2c1OC(C)=CC=C2 Chemical compound CC(C)(c1cc(Br)c2[o]c(C)nc2c1)c(cc1Br)cc2c1OC(C)=CC=C2 CBCICFOJVZPSPH-UHFFFAOYSA-N 0.000 description 1
- KRMORQNAJJDORZ-UHFFFAOYSA-N CC(CC1)CCC1(c1ccc(COC(C)=C)c(C)c1)c1ccc2OC(C)=C=Cc2c1 Chemical compound CC(CC1)CCC1(c1ccc(COC(C)=C)c(C)c1)c1ccc2OC(C)=C=Cc2c1 KRMORQNAJJDORZ-UHFFFAOYSA-N 0.000 description 1
- KYVORWODRINLOS-UHFFFAOYSA-N CC(c1cc(C=CC=C(C)C2)c2cc1)c1ccc(CCCC(C)=CC2=C)c2c1 Chemical compound CC(c1cc(C=CC=C(C)C2)c2cc1)c1ccc(CCCC(C)=CC2=C)c2c1 KYVORWODRINLOS-UHFFFAOYSA-N 0.000 description 1
- AWRJGBZLBLHRQQ-UHFFFAOYSA-N CC1=Nc2cc(C(c3ccccc3)(c3ccccc3)c3cc(N=C(C)C4OC44)c4cc3)ccc2OC1 Chemical compound CC1=Nc2cc(C(c3ccccc3)(c3ccccc3)c3cc(N=C(C)C4OC44)c4cc3)ccc2OC1 AWRJGBZLBLHRQQ-UHFFFAOYSA-N 0.000 description 1
- KOWFBENVHPWGLM-UHFFFAOYSA-N CCC(C)(C)c1cc(C(C)(C)CC)c(COc(cc2nc(C)[o]c2c2)c2[N+]([O-])=O)cc1 Chemical compound CCC(C)(C)c1cc(C(C)(C)CC)c(COc(cc2nc(C)[o]c2c2)c2[N+]([O-])=O)cc1 KOWFBENVHPWGLM-UHFFFAOYSA-N 0.000 description 1
- CTBVMKIQBIJMQL-UHFFFAOYSA-N CCC(C)C(OC1C(C2)C(CC3OC33)C3C2C1)=O Chemical compound CCC(C)C(OC1C(C2)C(CC3OC33)C3C2C1)=O CTBVMKIQBIJMQL-UHFFFAOYSA-N 0.000 description 1
- JTEXUYPZODUHAF-MODVXTFTSA-N CCCCC(CC)C/C=C(\CC)/CC(CC1)=CC(O2)=C1CC(C)(C1=C=Cc(cc(C(C)(C)c(cc3)cc4c3OC(C(C)(CC(C=CC(C)(C3)N(CC)CC(CC)CCCC)=C3O3)C3=O)N4)cc3)c3O1)C2=O Chemical compound CCCCC(CC)C/C=C(\CC)/CC(CC1)=CC(O2)=C1CC(C)(C1=C=Cc(cc(C(C)(C)c(cc3)cc4c3OC(C(C)(CC(C=CC(C)(C3)N(CC)CC(CC)CCCC)=C3O3)C3=O)N4)cc3)c3O1)C2=O JTEXUYPZODUHAF-MODVXTFTSA-N 0.000 description 1
- VCVCSPDUENKZBE-UHFFFAOYSA-N CCCCCCC(CCCC(CC)CCCC)c(cc1)cc(O2)c1C=C(c1nc(cc(cc3)-c(cc4)cc5c4[s]c(C4=Cc(ccc(N(CCCCCC)CC(CC)CCCC)c6)c6OC4=O)n5)c3[s]1)C2=O Chemical compound CCCCCCC(CCCC(CC)CCCC)c(cc1)cc(O2)c1C=C(c1nc(cc(cc3)-c(cc4)cc5c4[s]c(C4=Cc(ccc(N(CCCCCC)CC(CC)CCCC)c6)c6OC4=O)n5)c3[s]1)C2=O VCVCSPDUENKZBE-UHFFFAOYSA-N 0.000 description 1
- NDEVUDCRDHTGRK-UHFFFAOYSA-N CCOc(cc1)ccc1Oc(c([N+]([O-])=O)c1)cc2c1[o]c(C)n2 Chemical compound CCOc(cc1)ccc1Oc(c([N+]([O-])=O)c1)cc2c1[o]c(C)n2 NDEVUDCRDHTGRK-UHFFFAOYSA-N 0.000 description 1
- QHRZMGDJNNDMGZ-UHFFFAOYSA-N Cc1c(ccnc2)c2ccc1 Chemical compound Cc1c(ccnc2)c2ccc1 QHRZMGDJNNDMGZ-UHFFFAOYSA-N 0.000 description 1
- GZYWKAICTSFHRE-UHFFFAOYSA-N Cc1nc(cc(c([N+]([O-])=O)c2)Oc(cc3)ccc3O)c2[o]1 Chemical compound Cc1nc(cc(c([N+]([O-])=O)c2)Oc(cc3)ccc3O)c2[o]1 GZYWKAICTSFHRE-UHFFFAOYSA-N 0.000 description 1
- FPXVWFRBNCPQIA-UHFFFAOYSA-N Cc1nc(cc(cc2Br)S(c(cc3Br)cc4c3[o]c(C)n4)(=O)=O)c2[o]1 Chemical compound Cc1nc(cc(cc2Br)S(c(cc3Br)cc4c3[o]c(C)n4)(=O)=O)c2[o]1 FPXVWFRBNCPQIA-UHFFFAOYSA-N 0.000 description 1
- OSRIMXCCLFGVIB-UHFFFAOYSA-N Nc1cccc(S(c2cc(N=C(CC3)C4CCCCCC4)c3cc2)(=O)=O)c1 Chemical compound Nc1cccc(S(c2cc(N=C(CC3)C4CCCCCC4)c3cc2)(=O)=O)c1 OSRIMXCCLFGVIB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Optical Filters (AREA)
- Materials For Photolithography (AREA)
- Liquid Crystal (AREA)
- Plural Heterocyclic Compounds (AREA)
- Polymerisation Methods In General (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012282208A JP6098158B2 (ja) | 2011-12-26 | 2012-12-26 | 化合物 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011282956 | 2011-12-26 | ||
JP2011282956 | 2011-12-26 | ||
JP2012282208A JP6098158B2 (ja) | 2011-12-26 | 2012-12-26 | 化合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013151668A JP2013151668A (ja) | 2013-08-08 |
JP6098158B2 true JP6098158B2 (ja) | 2017-03-22 |
Family
ID=48632879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012282208A Active JP6098158B2 (ja) | 2011-12-26 | 2012-12-26 | 化合物 |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP6098158B2 (zh) |
KR (1) | KR102021024B1 (zh) |
CN (1) | CN103172626B (zh) |
TW (1) | TWI554509B (zh) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101992864B1 (ko) * | 2012-02-13 | 2019-06-25 | 스미또모 가가꾸 가부시키가이샤 | 착색 경화성 수지 조성물 |
JP6155076B2 (ja) * | 2012-04-10 | 2017-06-28 | 住友化学株式会社 | 着色剤分散液 |
WO2014208767A1 (ja) * | 2013-06-26 | 2014-12-31 | 住友化学株式会社 | 着色硬化性樹脂組成物 |
KR102031127B1 (ko) * | 2013-10-03 | 2019-10-11 | 동우 화인켐 주식회사 | 염료 분산액 |
JP6588688B2 (ja) * | 2014-03-27 | 2019-10-09 | 旭有機材株式会社 | 化合物、組成物及び硬化物 |
JP6347154B2 (ja) * | 2014-05-23 | 2018-06-27 | 大日本印刷株式会社 | 液晶表示装置およびカラーフィルタ |
JP6808921B2 (ja) * | 2014-10-30 | 2021-01-06 | 住友化学株式会社 | 化合物および着色硬化性樹脂組成物 |
JP6480728B2 (ja) * | 2014-12-26 | 2019-03-13 | 住友化学株式会社 | 化合物 |
JP6440494B2 (ja) * | 2014-12-26 | 2018-12-19 | 住友化学株式会社 | 化合物 |
WO2017010852A1 (ko) * | 2015-07-16 | 2017-01-19 | 에스에프씨 주식회사 | 염료 화합물 |
CN105777729A (zh) * | 2016-05-31 | 2016-07-20 | 浙江工业大学 | 一种香豆素酰胺类化合物及其制备方法和应用 |
CN106243093B (zh) * | 2016-07-19 | 2018-09-28 | 南京信息工程大学 | 双香豆素衍生物及其制备方法 |
CN107793407B (zh) * | 2016-09-06 | 2022-07-08 | 住友化学株式会社 | 作为着色剂有用的化合物 |
JP6821490B2 (ja) * | 2017-04-03 | 2021-01-27 | 日本化薬株式会社 | クマリン化合物又はそれらの塩、並びにこれを含んだ顔料組成物 |
KR102025478B1 (ko) * | 2017-11-28 | 2019-09-25 | 주식회사 엘지화학 | 착색제 조성물 제조방법, 이를 이용하여 제조된 착색제 조성물, 착색제 분산액, 감광성 수지 조성물, 컬러필터 및 액정 표시 장치 |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH390250A (de) * | 1958-06-19 | 1965-07-30 | Geigy Ag J R | Verfahren zur Herstellung von fluoreszierenden Farbstoffen |
DE2013262A1 (en) * | 1970-03-20 | 1971-10-07 | Badische Anilin & Soda Fabrik AG, 6700 Ludwigshafen | Acid gp-contg 3-(benzimidazolyl-2')-7-dialkyl amino cumarin |
US3985763A (en) * | 1970-06-20 | 1976-10-12 | Bayer Aktiengesellschaft | Oxazolyl-acetic acid derivatives and oxazolyl-coumarines |
JPS5142611B2 (zh) * | 1972-02-01 | 1976-11-17 | ||
JPS5529110B2 (zh) * | 1972-12-25 | 1980-08-01 | ||
EP0023022B1 (de) * | 1979-07-20 | 1984-04-11 | Ciba-Geigy Ag | Cumarinverbindungen, Verfahren zu deren Herstellung sowie die dafür verwendeten Zwischenprodukte an sich und ihre Verwendung zum Färben oder Bedrucken von Textilien |
US5199956A (en) * | 1990-09-03 | 1993-04-06 | Ciba-Geigy Corporation | Process for dyeing hydrophobic textile material with disperse dyes from super-critical carbon dioxide |
GB9404020D0 (en) * | 1994-03-02 | 1994-04-20 | Zeneca Ltd | Process |
DE19509043A1 (de) * | 1995-03-03 | 1996-09-05 | Bayer Ag | Cyanierung von Doppelbindungssystemen |
EP0879867B1 (en) * | 1996-02-09 | 2004-05-12 | Idemitsu Kosan Company Limited | Fluorescence-reddening membrane and red-emitting device |
JP3934729B2 (ja) * | 1996-03-29 | 2007-06-20 | 株式会社東芝 | 液晶表示素子 |
EP0827986B1 (de) * | 1996-09-05 | 2002-03-27 | Bayer Ag | Verbrückte Perinone, Chinophthalone und Perinon-Chinophthalone |
JP2001011079A (ja) * | 1999-04-27 | 2001-01-16 | Mitsubishi Chemicals Corp | クマリン系化合物、有機電界発光素子用色素及びこれを用いた有機電界発光素子 |
CN1111190C (zh) * | 2000-01-21 | 2003-06-11 | 大连理工大学 | 香豆素荧光染料 |
CA2417502C (en) * | 2000-07-27 | 2012-01-10 | Nippon Kayaku Kabushiki Kaisha | Dye-sensitized photoelectric conversion device |
DE10158137A1 (de) * | 2001-11-27 | 2003-05-28 | Bayer Ag | Verbrückte Perinone/Chinophthalone |
US7514158B2 (en) * | 2001-12-13 | 2009-04-07 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Coumarin compound |
US6770385B2 (en) * | 2002-01-09 | 2004-08-03 | Canon Inc. | Fluorescent bis-coumarins for organic light-emitting devices |
EP1547996A4 (en) * | 2002-08-30 | 2006-08-02 | Bf Res Inst Inc | DIAGNOSTIC PROBES AND REMEDIES FOR DISEASES HAVING PRION PROTEIN ACCUMULATION AND METHOD OF MARKING |
TWI245067B (en) * | 2002-12-18 | 2005-12-11 | Labeltek Inc | Coumarin derivative and EL element using the coumarin derivative |
KR100669717B1 (ko) * | 2004-07-29 | 2007-01-16 | 삼성에스디아이 주식회사 | 유기 전계 발광 소자 |
JP5221859B2 (ja) * | 2006-03-09 | 2013-06-26 | 株式会社Adeka | クマリン化合物を含有してなるフィルム、クマリン化合物とマトリクスを含む色変換層、該色変換層を含む色変換フィルタ、補色層、補色フィルタならびに多色発光デバイス |
JP5251329B2 (ja) * | 2008-07-22 | 2013-07-31 | 東洋インキScホールディングス株式会社 | カラーフィルタ用青色着色組成物、カラーフィルタおよびカラー表示装置 |
US8540521B2 (en) * | 2008-12-29 | 2013-09-24 | Life Technologies Corporation | Benzoxazole-based fluorescent metal ion indicators |
-
2012
- 2012-12-24 TW TW101149629A patent/TWI554509B/zh active
- 2012-12-24 KR KR1020120152296A patent/KR102021024B1/ko active IP Right Grant
- 2012-12-26 JP JP2012282208A patent/JP6098158B2/ja active Active
- 2012-12-26 CN CN201210576902.0A patent/CN103172626B/zh active Active
Also Published As
Publication number | Publication date |
---|---|
TW201331198A (zh) | 2013-08-01 |
JP2013151668A (ja) | 2013-08-08 |
KR20130079234A (ko) | 2013-07-10 |
CN103172626B (zh) | 2017-10-24 |
TWI554509B (zh) | 2016-10-21 |
CN103172626A (zh) | 2013-06-26 |
KR102021024B1 (ko) | 2019-09-11 |
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