JPS61197563A - トリフルオロメチルフエニル基をもつピリミジン誘導体 - Google Patents
トリフルオロメチルフエニル基をもつピリミジン誘導体Info
- Publication number
- JPS61197563A JPS61197563A JP60038328A JP3832885A JPS61197563A JP S61197563 A JPS61197563 A JP S61197563A JP 60038328 A JP60038328 A JP 60038328A JP 3832885 A JP3832885 A JP 3832885A JP S61197563 A JPS61197563 A JP S61197563A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- liquid crystal
- group
- pyrimidine derivative
- 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.)
- Granted
Links
- 150000003230 pyrimidines Chemical class 0.000 title claims abstract 4
- -1 trifluoromethylphenyl group Chemical group 0.000 title description 5
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 29
- 239000000203 mixture Substances 0.000 claims abstract description 17
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 32
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 13
- 239000000463 material Substances 0.000 abstract description 6
- 230000003247 decreasing effect Effects 0.000 abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003054 catalyst Substances 0.000 abstract description 2
- 239000007789 gas Substances 0.000 abstract description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract description 2
- RBJRBTHJFAJOJZ-UHFFFAOYSA-N 5-propyl-2-[4-(trifluoromethyl)phenyl]pyrimidine Chemical compound N1=CC(CCC)=CN=C1C1=CC=C(C(F)(F)F)C=C1 RBJRBTHJFAJOJZ-UHFFFAOYSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000007363 ring formation reaction Methods 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000012071 phase Substances 0.000 description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- DKIFMADLURULQV-UHFFFAOYSA-N 4-(trifluoromethyl)benzenecarboximidamide;hydrochloride Chemical compound Cl.NC(=N)C1=CC=C(C(F)(F)F)C=C1 DKIFMADLURULQV-UHFFFAOYSA-N 0.000 description 1
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical class C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical class C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3441—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
- C09K19/345—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing two nitrogen atoms
- C09K19/3458—Uncondensed pyrimidines
- C09K19/3469—Pyrimidine with a specific end-group other than alkyl, alkoxy or -C*-
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Liquid Crystal Substances (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60038328A JPS61197563A (ja) | 1985-02-27 | 1985-02-27 | トリフルオロメチルフエニル基をもつピリミジン誘導体 |
| US06/828,338 US4684476A (en) | 1985-02-27 | 1986-02-11 | Pyrimidine derivative and liquid crystal composition containing same |
| DE8686102533T DE3665585D1 (en) | 1985-02-27 | 1986-02-27 | Pyrimidine derivative and liquid crystal composition containing same |
| EP86102533A EP0193191B1 (en) | 1985-02-27 | 1986-02-27 | Pyrimidine derivative and liquid crystal composition containing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60038328A JPS61197563A (ja) | 1985-02-27 | 1985-02-27 | トリフルオロメチルフエニル基をもつピリミジン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61197563A true JPS61197563A (ja) | 1986-09-01 |
| JPH0578546B2 JPH0578546B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-10-29 |
Family
ID=12522213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60038328A Granted JPS61197563A (ja) | 1985-02-27 | 1985-02-27 | トリフルオロメチルフエニル基をもつピリミジン誘導体 |
Country Status (4)
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01503145A (ja) * | 1987-04-28 | 1989-10-26 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 電気光学表示素子 |
| JPH0415290A (ja) * | 1990-05-09 | 1992-01-20 | Canon Inc | カイラルスメクチック液晶組成物およびそれを使用した液晶素子 |
| WO1998017664A1 (fr) * | 1996-10-22 | 1998-04-30 | Chisso Corporation | Derives de dioxane, compositions de cristaux liquides contenant ces derives, et dispositif d'affichage a cristaux liquides fabrique a partir de ces derniers |
| US7001647B2 (en) | 2002-12-24 | 2006-02-21 | Asahi Denka Co., Ltd. | Perfluoroallyloxy compound and liquid crystal composition containing the same |
| DE112006001453T5 (de) | 2005-06-09 | 2008-11-06 | Adeka Corp. | Neue Verbindung und Flüssigkristall-Zusammensetzung |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3315295A1 (de) * | 1983-04-27 | 1984-10-31 | Merck Patent Gmbh, 6100 Darmstadt | Fluorhaltige pyrimidinderivate |
| EP0225195B1 (en) * | 1985-12-04 | 1993-11-24 | Ajinomoto Co., Inc. | Phenylpyrimidine-based compounds and liquid crystal composition containing the same |
| DE3614778A1 (de) * | 1986-05-02 | 1987-11-05 | Merck Patent Gmbh | Smektische fluessigkristalline phasen |
| DE3852422T2 (de) * | 1987-04-27 | 1995-05-04 | Chisso Corp | Optisch aktive 2-Biphenylpyrimidinderivate und diese enthaltende Flüssigkristallmischungen. |
| JPH0730041B2 (ja) * | 1987-06-01 | 1995-04-05 | チッソ株式会社 | スメクチック性液晶化合物 |
| US5324449A (en) * | 1987-09-25 | 1994-06-28 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Substituted phenyl trifluoromethyl ethers |
| US5536442A (en) * | 1987-09-25 | 1996-07-16 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Fluorinated liquid crystal compounds and liquid crystal medium containing same |
| DE3909802A1 (de) * | 1988-07-27 | 1990-04-05 | Merck Patent Gmbh | Difluormethylverbindungen |
| DE3884347T2 (de) * | 1987-11-17 | 1994-04-28 | Seiko Epson Corp | Pyrimidinderivate. |
| DE3930119A1 (de) * | 1989-04-08 | 1990-10-11 | Merck Patent Gmbh | Trifluormethylcyclohexan-derivate |
| DE3928267A1 (de) * | 1989-08-26 | 1991-02-28 | Merck Patent Gmbh | 5-oxy-2-phenylpyrimidine und fluessigkristallines medium |
| US5308542A (en) * | 1990-03-13 | 1994-05-03 | Merck Patent Gesellschaft Mit Beschrankter Haftung | 4,4'-disubstituted 2',3-difluorobisphenyls and a liquid-crystalline medium |
| DE59108187D1 (de) * | 1990-04-13 | 1996-10-24 | Merck Patent Gmbh | Flüssigkristallines Medium |
| DE4107167B4 (de) * | 1991-03-06 | 2008-05-08 | Merck Patent Gmbh | Flüssigkristallmischung |
| DE4217248B4 (de) * | 1991-06-05 | 2005-06-16 | Merck Patent Gmbh | Vinylverbindungen |
| EP0519370B1 (en) * | 1991-06-21 | 1997-11-05 | MERCK PATENT GmbH | Heterocyclic derivatives |
| JP3049681B2 (ja) * | 1993-09-17 | 2000-06-05 | キヤノン株式会社 | 液晶性化合物、それを含有する液晶組成物、それを有する液晶素子及びそれらを用いた表示方法、表示装置 |
| JPH1129557A (ja) * | 1997-07-08 | 1999-02-02 | Chisso Corp | ピリミジン誘導体、これを含む液晶組成物およびこれを用いた液晶表示素子 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE144423C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | ||||
| US4011173A (en) * | 1972-08-03 | 1977-03-08 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Modified nematic mixtures with positive dielectric anisotropy |
| CH617452A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1974-10-25 | 1980-05-30 | Hoffmann La Roche | |
| US4062798A (en) * | 1975-09-19 | 1977-12-13 | Hoffmann-La Roche Inc. | Phenylpyrimidine derivatives |
| DE3014912A1 (de) * | 1979-05-15 | 1980-11-27 | Werk Fernsehelektronik Veb | Nematische fluessigkristalline 5-cyan- 2- eckige klammer auf 4-acyloxyphenyl eckige klammer zu -pyrimidine und diese enthaltende gemische |
| DE2927277A1 (de) * | 1979-07-06 | 1981-01-08 | Merck Patent Gmbh | Cyclohexylbiphenyle, verfahren zu ihrer herstellung, diese enthaltende dielektrika und elektrooptisches anzeigeelement |
| DD144423A1 (de) * | 1979-08-20 | 1980-10-15 | Horst Zaschke | Nematische kristallin-fluessige substanzen |
| DE3063497D1 (en) * | 1979-08-20 | 1983-07-07 | Werk Fernsehelektronik Veb | Nematic crystalline-liquid 5-alkyl-2-(4-acyloxyphenyl)-pyrimidines for opto-electronic arrangements and process for their preparation |
| DE2951099A1 (de) * | 1979-12-19 | 1981-06-25 | Merck Patent Gmbh, 6100 Darmstadt | Tetrahydrochinazoline, verfahren zu ihrer herstellung, diese enthaltende fluessigkristalline dielektrika und elektrooptisches anzeigeelement |
| DE3006666A1 (de) * | 1980-02-22 | 1981-09-17 | Merck Patent Gmbh, 6100 Darmstadt | Phenylcyclohexenderivate, verfahren zu ihrer herstellung, diese enthaltende fluessigkristalline dielektrika und elektrooptisches anzeieelement |
| EP0056501B1 (de) * | 1981-01-19 | 1984-05-02 | MERCK PATENT GmbH | Flüssigkristallmischung |
| DE3270906D1 (en) * | 1982-01-14 | 1986-06-05 | Merck Patent Gmbh | Liquid crystal mixtures |
| JPS58198427A (ja) * | 1982-05-13 | 1983-11-18 | Chisso Corp | ４−〔４′−（トランス−４″−アルキルシクロヘキシル）シクロヘキセン−１′−イル〕ベンゾトリフルオロメタン |
| DE3407013A1 (de) * | 1984-02-27 | 1985-09-05 | Merck Patent Gmbh, 6100 Darmstadt | Cyclohexanderivate |
| JPS5939876A (ja) * | 1982-08-26 | 1984-03-05 | Chisso Corp | ピリミジン誘導体 |
| JPS6054371A (ja) * | 1983-09-01 | 1985-03-28 | Chisso Corp | ５−アルキル−２−（置換フエニル）ピリミジン |
| JPS59216876A (ja) * | 1983-05-24 | 1984-12-06 | Chisso Corp | フルオロピリミジン誘導体 |
| US4581155A (en) * | 1983-03-31 | 1986-04-08 | Chisso Corporation | Halogenopyrimidine derivatives |
| DE3315295A1 (de) * | 1983-04-27 | 1984-10-31 | Merck Patent Gmbh, 6100 Darmstadt | Fluorhaltige pyrimidinderivate |
| DE3401321A1 (de) * | 1984-01-17 | 1985-07-25 | Merck Patent Gmbh, 6100 Darmstadt | Stickstoffhaltige heterocyclen |
| DE3404116A1 (de) * | 1984-02-07 | 1985-08-08 | Merck Patent Gmbh, 6100 Darmstadt | Stickstoffhaltige heterocyclen |
| US4640795A (en) * | 1986-03-21 | 1987-02-03 | Chisso Corporation | 5-alkyl-2-(3,4-difluorophenyl)pyrimidine and nematic liquid crystal composition containing same |
-
1985
- 1985-02-27 JP JP60038328A patent/JPS61197563A/ja active Granted
-
1986
- 1986-02-11 US US06/828,338 patent/US4684476A/en not_active Expired - Fee Related
- 1986-02-27 DE DE8686102533T patent/DE3665585D1/de not_active Expired
- 1986-02-27 EP EP86102533A patent/EP0193191B1/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01503145A (ja) * | 1987-04-28 | 1989-10-26 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 電気光学表示素子 |
| JPH0415290A (ja) * | 1990-05-09 | 1992-01-20 | Canon Inc | カイラルスメクチック液晶組成物およびそれを使用した液晶素子 |
| WO1998017664A1 (fr) * | 1996-10-22 | 1998-04-30 | Chisso Corporation | Derives de dioxane, compositions de cristaux liquides contenant ces derives, et dispositif d'affichage a cristaux liquides fabrique a partir de ces derniers |
| US7001647B2 (en) | 2002-12-24 | 2006-02-21 | Asahi Denka Co., Ltd. | Perfluoroallyloxy compound and liquid crystal composition containing the same |
| DE112006001453T5 (de) | 2005-06-09 | 2008-11-06 | Adeka Corp. | Neue Verbindung und Flüssigkristall-Zusammensetzung |
| US7785675B2 (en) | 2005-06-09 | 2010-08-31 | Adeka Corporation | Compound and liquid crystal composition |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3665585D1 (en) | 1989-10-19 |
| EP0193191B1 (en) | 1989-09-13 |
| US4684476A (en) | 1987-08-04 |
| JPH0578546B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-10-29 |
| EP0193191A2 (en) | 1986-09-03 |
| EP0193191A3 (en) | 1986-12-30 |