JPH0150692B2 - - Google Patents
Info
- Publication number
- JPH0150692B2 JPH0150692B2 JP10003981A JP10003981A JPH0150692B2 JP H0150692 B2 JPH0150692 B2 JP H0150692B2 JP 10003981 A JP10003981 A JP 10003981A JP 10003981 A JP10003981 A JP 10003981A JP H0150692 B2 JPH0150692 B2 JP H0150692B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- trans
- cyclohexanecarboxylic acid
- substituted phenyl
- chlorophenyl ester
- 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.)
- Expired
Links
- 239000004973 liquid crystal related substance Substances 0.000 claims description 16
- -1 trans-4-(4'-substituted phenyl) -Cyclohexanecarboxylic acid Chemical class 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 claims 2
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 210000002858 crystal cell Anatomy 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- WLPATYNQCGVFFH-UHFFFAOYSA-N 2-phenylbenzonitrile Chemical group N#CC1=CC=CC=C1C1=CC=CC=C1 WLPATYNQCGVFFH-UHFFFAOYSA-N 0.000 description 1
- ZGOWXOZNUNZPAV-UHFFFAOYSA-N 4-(4-heptylphenyl)benzonitrile Chemical group C1=CC(CCCCCCC)=CC=C1C1=CC=C(C#N)C=C1 ZGOWXOZNUNZPAV-UHFFFAOYSA-N 0.000 description 1
- GPGGNNIMKOVSAG-UHFFFAOYSA-N 4-(4-octoxyphenyl)benzonitrile Chemical group C1=CC(OCCCCCCCC)=CC=C1C1=CC=C(C#N)C=C1 GPGGNNIMKOVSAG-UHFFFAOYSA-N 0.000 description 1
- PBMCTXQDYLSLTP-UHFFFAOYSA-N 4-(4-pentylphenyl)-3-phenylbenzonitrile Chemical group C1=CC(CCCCC)=CC=C1C1=CC=C(C#N)C=C1C1=CC=CC=C1 PBMCTXQDYLSLTP-UHFFFAOYSA-N 0.000 description 1
- YOXTXHPMOBOZQO-UHFFFAOYSA-N 4-(4-propylphenyl)cyclohexane-1-carboxylic acid Chemical compound C1=CC(CCC)=CC=C1C1CCC(C(O)=O)CC1 YOXTXHPMOBOZQO-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10003981A JPS584745A (ja) | 1981-06-27 | 1981-06-27 | トランス−４−（４′−置換フエニル）−シクロヘキサンカルボン酸４″−クロロフエニルエステル |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10003981A JPS584745A (ja) | 1981-06-27 | 1981-06-27 | トランス−４−（４′−置換フエニル）−シクロヘキサンカルボン酸４″−クロロフエニルエステル |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS584745A JPS584745A (ja) | 1983-01-11 |
| JPH0150692B2 true JPH0150692B2 (en]) | 1989-10-31 |
Family
ID=14263376
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10003981A Granted JPS584745A (ja) | 1981-06-27 | 1981-06-27 | トランス−４−（４′−置換フエニル）−シクロヘキサンカルボン酸４″−クロロフエニルエステル |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS584745A (en]) |
-
1981
- 1981-06-27 JP JP10003981A patent/JPS584745A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS584745A (ja) | 1983-01-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6144863B2 (en]) | ||
| US4585575A (en) | 2-substituted-6-(5-substituted-2-pyrimidinyl)naphthalenes | |
| JPS58121272A (ja) | ３−クロロ−６−ヒドロキシピリジンのエステル誘導体 | |
| JPH0331184B2 (en]) | ||
| JPH0150692B2 (en]) | ||
| JPS58126839A (ja) | ４−（トランス−４′−アルキルシクロヘキシル）安息香酸２，４−ジハロゲノフエニルエステル | |
| JP2633314B2 (ja) | アルケニルオキシ安息酸ハロゲノビフェニルエステル | |
| JPH0246027B2 (en]) | ||
| JPH0320378B2 (en]) | ||
| JPH0131499B2 (en]) | ||
| JPS60237048A (ja) | エステル化合物 | |
| JPH0565236A (ja) | フルオロトラン系アルケニル化合物 | |
| JPH055821B2 (en]) | ||
| JP2500687B2 (ja) | ビシクロヘキシルトラン誘導体 | |
| JPH0233696B2 (ja) | Shianoshikurohekisanjudotai | |
| JP2822083B2 (ja) | アルキンオキシフエニルビシクロヘキサン類化合物 | |
| JPS60246347A (ja) | 安息香酸フエネチルエステル誘導体 | |
| JPH037653B2 (en]) | ||
| JPS642595B2 (en]) | ||
| JPH04360890A (ja) | ケイ素液晶化合物 | |
| JPS58203963A (ja) | トランス−４−（４′−置換フエニル）シクロヘキサンカルボン酸−４−フルオロチオフエニルエステル | |
| JPH01193254A (ja) | アリルピリミジニルフェノールのエステル誘導体 | |
| JPH0210817B2 (en]) | ||
| JPH0142261B2 (en]) | ||
| JPH0558958A (ja) | フツ素液晶化合物 |