JPH0329058B2 - - Google Patents
Info
- Publication number
- JPH0329058B2 JPH0329058B2 JP4042683A JP4042683A JPH0329058B2 JP H0329058 B2 JPH0329058 B2 JP H0329058B2 JP 4042683 A JP4042683 A JP 4042683A JP 4042683 A JP4042683 A JP 4042683A JP H0329058 B2 JPH0329058 B2 JP H0329058B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- liquid crystal
- present
- viscosity
- phase
- 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 24
- 239000000203 mixture Substances 0.000 claims description 12
- -1 3-trifluoromethylphenyl group Chemical group 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000126 substance Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UGEJOEBBMPOJMT-UHFFFAOYSA-N 3-(trifluoromethyl)phenol Chemical compound OC1=CC=CC(C(F)(F)F)=C1 UGEJOEBBMPOJMT-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004990 Smectic liquid crystal Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 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
- HHPCNRKYVYWYAU-UHFFFAOYSA-N 4-cyano-4'-pentylbiphenyl Chemical group C1=CC(CCCCC)=CC=C1C1=CC=C(C#N)C=C1 HHPCNRKYVYWYAU-UHFFFAOYSA-N 0.000 description 1
- FLJRBFMGAYFGNF-VVPTUSLJSA-N C(CCCCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)C(=O)O Chemical compound C(CCCCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)C(=O)O FLJRBFMGAYFGNF-VVPTUSLJSA-N 0.000 description 1
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 1
- 239000004988 Nematic liquid crystal Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4042683A JPS59167540A (ja) | 1983-03-11 | 1983-03-11 | エステル誘導体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4042683A JPS59167540A (ja) | 1983-03-11 | 1983-03-11 | エステル誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59167540A JPS59167540A (ja) | 1984-09-21 |
| JPH0329058B2 true JPH0329058B2 (de) | 1991-04-23 |
Family
ID=12580322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4042683A Granted JPS59167540A (ja) | 1983-03-11 | 1983-03-11 | エステル誘導体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59167540A (de) |
-
1983
- 1983-03-11 JP JP4042683A patent/JPS59167540A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59167540A (ja) | 1984-09-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6168467A (ja) | 正の誘電異方性を有するエステル誘導体 | |
| JPS60255779A (ja) | 複素環化合物 | |
| US4534883A (en) | 4-Unsubstituted or substituted-4 cyanotercyclohexane derivatives | |
| JPS59141540A (ja) | 三環カルボン酸エステル誘導体 | |
| JPH0329058B2 (de) | ||
| JPS59157056A (ja) | 光学活性アルコ−ルのエステル | |
| JPH055821B2 (de) | ||
| JPS60197637A (ja) | β−（４−置換フエニル）プロピオン酸フエニルエステル誘導体 | |
| JPS60199867A (ja) | α−メチル−β−（４−置換フエニル）プロピオン酸のシアノフエニルエステル誘導体 | |
| JPH037653B2 (de) | ||
| JPS61282345A (ja) | エステル化合物 | |
| JPS615054A (ja) | シクロヘキサンカルボン酸フエネチルエステル誘導体 | |
| JPS60181059A (ja) | β−（４−置換フエニル）プロピオン酸のシアノフエニルエステル誘導体 | |
| JPH0233696B2 (ja) | Shianoshikurohekisanjudotai | |
| JPH0443897B2 (de) | ||
| JPS60188347A (ja) | α−メチル−β−（４−置換フエニル）プロピオン酸のハロゲノフエニルのエステル誘導体 | |
| JPS60204743A (ja) | β−（４−置換フエニル）プロピオン酸のハロゲノフエニルエステル誘導体 | |
| JPS62138471A (ja) | ピリジン誘導体 | |
| JPH0142941B2 (de) | ||
| JPS59196854A (ja) | ４−アルキル−２−シアノフエノ−ルのエステル類 | |
| JPS59144748A (ja) | ４−ヒドロキシ−３−メトキシベンゾニトリルのエステル | |
| JPS59161333A (ja) | メタ置換フエノ−ルのエステル誘導体 | |
| JPS58210047A (ja) | ２，４−ジクロロ安息香酸−４−（トランス−４′−アルキルシクロヘキシル）フエニルエステル | |
| JPH0358334B2 (de) | ||
| JPH0142260B2 (de) |