JPS5955864A - オルトシアノフエノ−ルのエステル - Google Patents
オルトシアノフエノ−ルのエステルInfo
- Publication number
- JPS5955864A JPS5955864A JP16817482A JP16817482A JPS5955864A JP S5955864 A JPS5955864 A JP S5955864A JP 16817482 A JP16817482 A JP 16817482A JP 16817482 A JP16817482 A JP 16817482A JP S5955864 A JPS5955864 A JP S5955864A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- trans
- cyano
- chlorophenol
- 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 description 3
- CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 title 1
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 11
- -1 trans-4-substituted cyclohexanecarboxylic acid chloride Chemical class 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N Cyclohexanecarboxylic acid Natural products OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 claims 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract description 4
- XWQDMIXVAYAZGB-UHFFFAOYSA-N 5-chloro-2-hydroxybenzonitrile Chemical compound OC1=CC=C(Cl)C=C1C#N XWQDMIXVAYAZGB-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004988 Nematic liquid crystal Substances 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 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 2
- 239000013078 crystal Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- PRCPBWAVIZAFQH-UHFFFAOYSA-N (2-formylphenyl) hypochlorite Chemical compound ClOC1=CC=CC=C1C=O PRCPBWAVIZAFQH-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
- 239000002253 acid Substances 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
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 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)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Liquid Crystal (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16817482A JPS5955864A (ja) | 1982-09-27 | 1982-09-27 | オルトシアノフエノ−ルのエステル |
US06/530,786 US4603018A (en) | 1982-09-27 | 1983-09-09 | 2-cyano-4-halogenophenyl esters |
EP83305765A EP0106588B1 (en) | 1982-09-27 | 1983-09-27 | 2-cyano-4-halogenophenyl esters |
DE8383305765T DE3363290D1 (de) | 1982-09-27 | 1983-09-27 | 2-cyano-4-halogenophenyl esters |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16817482A JPS5955864A (ja) | 1982-09-27 | 1982-09-27 | オルトシアノフエノ−ルのエステル |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5955864A true JPS5955864A (ja) | 1984-03-31 |
JPS64386B2 JPS64386B2 (enrdf_load_stackoverflow) | 1989-01-06 |
Family
ID=15863163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16817482A Granted JPS5955864A (ja) | 1982-09-27 | 1982-09-27 | オルトシアノフエノ−ルのエステル |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5955864A (enrdf_load_stackoverflow) |
-
1982
- 1982-09-27 JP JP16817482A patent/JPS5955864A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS64386B2 (enrdf_load_stackoverflow) | 1989-01-06 |