JPS6338987B2 - - Google Patents
Info
- Publication number
- JPS6338987B2 JPS6338987B2 JP164481A JP164481A JPS6338987B2 JP S6338987 B2 JPS6338987 B2 JP S6338987B2 JP 164481 A JP164481 A JP 164481A JP 164481 A JP164481 A JP 164481A JP S6338987 B2 JPS6338987 B2 JP S6338987B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- ester
- dicyan
- ethenyl
- acid
- 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
- 239000000203 mixture Substances 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 14
- 239000004988 Nematic liquid crystal Substances 0.000 claims description 6
- FNCOVSWSZZVFBQ-UHFFFAOYSA-N 2-[(4-hydroxyphenyl)methylidene]propanedinitrile Chemical compound OC1=CC=C(C=C(C#N)C#N)C=C1 FNCOVSWSZZVFBQ-UHFFFAOYSA-N 0.000 claims description 4
- -1 4-substituted-benzoic acid Chemical class 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 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 claims description 2
- CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims 3
- 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
- 239000000463 material Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 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
- SSYVIRDHEJGVCM-UHFFFAOYSA-N (4-carbonochloridoylphenyl) heptanoate Chemical compound CCCCCCC(=O)OC1=CC=C(C(Cl)=O)C=C1 SSYVIRDHEJGVCM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- OIBFRBIJSBWAHB-UHFFFAOYSA-N (2-butoxyphenyl) 2-hexylbenzoate Chemical compound CCCCCCC1=CC=CC=C1C(=O)OC1=CC=CC=C1OCCCC OIBFRBIJSBWAHB-UHFFFAOYSA-N 0.000 description 1
- SNHILALQOKRTCZ-UHFFFAOYSA-N (2-hexoxyphenyl) 2-butoxycarbonyloxybenzoate Chemical compound CCCCCCOC1=CC=CC=C1OC(=O)C1=CC=CC=C1OC(=O)OCCCC SNHILALQOKRTCZ-UHFFFAOYSA-N 0.000 description 1
- CHEWMQGNEABRHZ-UHFFFAOYSA-N (2-hexoxyphenyl) 2-methoxybenzoate Chemical compound CCCCCCOC1=CC=CC=C1OC(=O)C1=CC=CC=C1OC CHEWMQGNEABRHZ-UHFFFAOYSA-N 0.000 description 1
- BADVPHQPIAWXCD-UHFFFAOYSA-N (2-octoxyphenyl) 2-pentoxybenzoate Chemical compound CCCCCCCCOC1=CC=CC=C1OC(=O)C1=CC=CC=C1OCCCCC BADVPHQPIAWXCD-UHFFFAOYSA-N 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 210000004681 ovum Anatomy 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Liquid Crystal Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD21841080A DD158177A3 (de) | 1980-01-11 | 1980-01-11 | Kristallin-fluessige nematische gemische |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56104985A JPS56104985A (en) | 1981-08-21 |
| JPS6338987B2 true JPS6338987B2 (enExample) | 1988-08-03 |
Family
ID=5522216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP164481A Granted JPS56104985A (en) | 1980-01-11 | 1981-01-10 | Liquid crystal composition of 44*2*22dicyannethenyl**phenol ester |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS56104985A (enExample) |
| DD (1) | DD158177A3 (enExample) |
| HU (1) | HU190670B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH647230A5 (en) * | 1981-06-18 | 1985-01-15 | Hoffmann La Roche | Phenyl esters, and the use thereof as components of liquid-crystalline mixtures |
| CN105637038B (zh) * | 2013-12-05 | 2019-10-25 | 株式会社艾迪科 | 新型化合物及含有该化合物的组合物 |
-
1980
- 1980-01-11 DD DD21841080A patent/DD158177A3/de not_active IP Right Cessation
-
1981
- 1981-01-09 HU HU5181A patent/HU190670B/hu not_active IP Right Cessation
- 1981-01-10 JP JP164481A patent/JPS56104985A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| HU190670B (en) | 1986-10-28 |
| JPS56104985A (en) | 1981-08-21 |
| DD158177A3 (de) | 1983-01-05 |
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