JPS6013731A - 置換フエニルエ−テル化合物 - Google Patents
置換フエニルエ−テル化合物Info
- Publication number
- JPS6013731A JPS6013731A JP11998383A JP11998383A JPS6013731A JP S6013731 A JPS6013731 A JP S6013731A JP 11998383 A JP11998383 A JP 11998383A JP 11998383 A JP11998383 A JP 11998383A JP S6013731 A JPS6013731 A JP S6013731A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- compound
- substituted phenyl
- trans
- 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
- -1 phenyl ether compound Chemical class 0.000 title claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 6
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 239000011737 fluorine Substances 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
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 25
- 150000001875 compounds Chemical class 0.000 abstract description 21
- 239000000463 material Substances 0.000 abstract description 12
- 239000004988 Nematic liquid crystal Substances 0.000 abstract description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 5
- 238000010992 reflux Methods 0.000 abstract description 4
- 239000011541 reaction mixture Substances 0.000 abstract description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LNEMDIUSUQPKIP-UHFFFAOYSA-N 2-phenyl-1,3-dioxane Chemical compound O1CCCOC1C1=CC=CC=C1 LNEMDIUSUQPKIP-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 210000004460 N cell Anatomy 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 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
- 239000002253 acid Substances 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
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- VJCWGXGMXAVKJU-UHFFFAOYSA-N cyclohexyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1CCCCC1 VJCWGXGMXAVKJU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- OPYYWWIJPHKUDZ-UHFFFAOYSA-N phenyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1=CC=CC=C1 OPYYWWIJPHKUDZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012485 toluene extract Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Liquid Crystal Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11998383A JPS6013731A (ja) | 1983-07-01 | 1983-07-01 | 置換フエニルエ−テル化合物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11998383A JPS6013731A (ja) | 1983-07-01 | 1983-07-01 | 置換フエニルエ−テル化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6013731A true JPS6013731A (ja) | 1985-01-24 |
| JPH0460976B2 JPH0460976B2 (enrdf_load_stackoverflow) | 1992-09-29 |
Family
ID=14774999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11998383A Granted JPS6013731A (ja) | 1983-07-01 | 1983-07-01 | 置換フエニルエ−テル化合物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6013731A (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4668427A (en) * | 1984-09-04 | 1987-05-26 | Chisso Corporation | Liquid crystal compound having methyleneoxy group and composition containing same |
| US4710315A (en) * | 1984-04-16 | 1987-12-01 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Anisotropic compounds and liquid crystal mixtures therewith |
| US4797228A (en) * | 1985-06-10 | 1989-01-10 | Chisso Corporation | Cyclohexane derivative and liquid crystal composition containing same |
| US5230826A (en) * | 1987-11-06 | 1993-07-27 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5780485A (en) * | 1980-11-07 | 1982-05-20 | Daido Steel Co Ltd | Controlling method in treatment for melting industrial waste or the like |
-
1983
- 1983-07-01 JP JP11998383A patent/JPS6013731A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5780485A (en) * | 1980-11-07 | 1982-05-20 | Daido Steel Co Ltd | Controlling method in treatment for melting industrial waste or the like |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4710315A (en) * | 1984-04-16 | 1987-12-01 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Anisotropic compounds and liquid crystal mixtures therewith |
| JPH0764767B2 (ja) * | 1984-04-16 | 1995-07-12 | 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 | 異方性化合物およびそれらを用いた液晶混合物 |
| USRE36849E (en) * | 1984-04-16 | 2000-09-05 | Merck Patent Gmbh | Anisotropic compounds and liquid crystal mixtures therewith |
| US4668427A (en) * | 1984-09-04 | 1987-05-26 | Chisso Corporation | Liquid crystal compound having methyleneoxy group and composition containing same |
| US4751019A (en) * | 1984-09-04 | 1988-06-14 | Chisso Corporation | Liquid crystal compound having methyleneoxy group and composition containing same |
| US4797228A (en) * | 1985-06-10 | 1989-01-10 | Chisso Corporation | Cyclohexane derivative and liquid crystal composition containing same |
| US4917819A (en) * | 1985-06-10 | 1990-04-17 | Chisso Corporation | Cyclohexane derivative and liquid crystal composition containing same |
| US5230826A (en) * | 1987-11-06 | 1993-07-27 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| US5302317A (en) * | 1987-11-06 | 1994-04-12 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| US5454974A (en) * | 1987-11-06 | 1995-10-03 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0460976B2 (enrdf_load_stackoverflow) | 1992-09-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH01216967A (ja) | 液晶化合物 | |
| JPS6013731A (ja) | 置換フエニルエ−テル化合物 | |
| JPS59216876A (ja) | フルオロピリミジン誘導体 | |
| JPS643858B2 (enrdf_load_stackoverflow) | ||
| JPS58167535A (ja) | トランス，トランス−４−アルキル−４′−アルキルオキシメチルビシクロヘキサン類 | |
| JP2829436B2 (ja) | シクロブタン誘導体 | |
| JPS58121272A (ja) | ３−クロロ−６−ヒドロキシピリジンのエステル誘導体 | |
| JPS60204769A (ja) | ハロゲノピリミジン誘導体 | |
| JPS5933566B2 (ja) | １，４−ジ−（シクロヘキシルエチル）ビフエニル誘導体 | |
| JP2822079B2 (ja) | シクロプロパン誘導体 | |
| JPS59170030A (ja) | 液晶性化合物 | |
| JPH03279340A (ja) | エーテル系３環式液晶化合物 | |
| JPS62138471A (ja) | ピリジン誘導体 | |
| JPS642595B2 (enrdf_load_stackoverflow) | ||
| JPS6059223B2 (ja) | 液晶性化合物 | |
| JP2773055B2 (ja) | ジアルキルフエニルビシクロヘキサン誘導体 | |
| JP3237025B2 (ja) | エ−テル誘導体液晶化合物 | |
| JP2508166B2 (ja) | 新規シクロヘキセニルシクロヘキサン誘導体 | |
| JPH0588692B2 (enrdf_load_stackoverflow) | ||
| JPS6168447A (ja) | フエノオキシ酢酸エステル誘導体 | |
| JPS58148875A (ja) | ４−（トランス−５−アルキル−１，３−ジオキサ−２−イル）安息香酸エステル誘導体 | |
| JPH0119391B2 (enrdf_load_stackoverflow) | ||
| JPS63267759A (ja) | ビフエニルピリジン誘導体 | |
| JPS6383069A (ja) | ２−（３−フルオロ−４−シアノフエニル）ピリジン誘導体 | |
| JPH0118906B2 (enrdf_load_stackoverflow) |