JPS59152364A - 負の誘電異方性値を持つエステル類 - Google Patents
負の誘電異方性値を持つエステル類Info
- Publication number
- JPS59152364A JPS59152364A JP2568883A JP2568883A JPS59152364A JP S59152364 A JPS59152364 A JP S59152364A JP 2568883 A JP2568883 A JP 2568883A JP 2568883 A JP2568883 A JP 2568883A JP S59152364 A JPS59152364 A JP S59152364A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- cyano
- ester
- 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
- 150000002148 esters Chemical class 0.000 title claims abstract description 8
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000004185 ester group Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 15
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract description 6
- 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 abstract description 4
- -1 cyclohexanecarboxylic acid alpha-cyano-4-butylphenyl ester Chemical class 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004988 Nematic liquid crystal Substances 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- NZNMSOFKMUBTKW-UHFFFAOYSA-N Cyclohexanecarboxylic acid Natural products OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 abstract 1
- 229910006124 SOCl2 Inorganic materials 0.000 abstract 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- HYYPJDROBJCKRW-HDRKRICHSA-N COC[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)C(=O)O Chemical compound COC[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)C(=O)O HYYPJDROBJCKRW-HDRKRICHSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CYURSYQPPHRSMN-UHFFFAOYSA-N 5-butyl-2-hydroxybenzonitrile Chemical compound CCCCC1=CC=C(O)C(C#N)=C1 CYURSYQPPHRSMN-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
- 239000000470 constituent Substances 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000003756 stirring 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 |
|---|---|---|---|
| JP2568883A JPS59152364A (ja) | 1983-02-18 | 1983-02-18 | 負の誘電異方性値を持つエステル類 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2568883A JPS59152364A (ja) | 1983-02-18 | 1983-02-18 | 負の誘電異方性値を持つエステル類 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59152364A true JPS59152364A (ja) | 1984-08-31 |
| JPH0326184B2 JPH0326184B2 (en, 2012) | 1991-04-10 |
Family
ID=12172725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2568883A Granted JPS59152364A (ja) | 1983-02-18 | 1983-02-18 | 負の誘電異方性値を持つエステル類 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59152364A (en, 2012) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57192351A (en) * | 1981-05-20 | 1982-11-26 | Chisso Corp | Trans-4-(trans-4'-alkylcyclohexyl)cyclohexanecarboxylic acid 2-cyanophenyl ester |
| US4368135A (en) * | 1979-07-18 | 1983-01-11 | Bbc, Brown, Boveri & Company, Ltd. | Anisotropic compounds with negative or positive DC-anisotropy and low optical anisotropy |
-
1983
- 1983-02-18 JP JP2568883A patent/JPS59152364A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4368135A (en) * | 1979-07-18 | 1983-01-11 | Bbc, Brown, Boveri & Company, Ltd. | Anisotropic compounds with negative or positive DC-anisotropy and low optical anisotropy |
| JPS57192351A (en) * | 1981-05-20 | 1982-11-26 | Chisso Corp | Trans-4-(trans-4'-alkylcyclohexyl)cyclohexanecarboxylic acid 2-cyanophenyl ester |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0326184B2 (en, 2012) | 1991-04-10 |
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