JPS642595B2 - - Google Patents
Info
- Publication number
- JPS642595B2 JPS642595B2 JP6037884A JP6037884A JPS642595B2 JP S642595 B2 JPS642595 B2 JP S642595B2 JP 6037884 A JP6037884 A JP 6037884A JP 6037884 A JP6037884 A JP 6037884A JP S642595 B2 JPS642595 B2 JP S642595B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- compound
- trans
- benzoic acid
- point
- 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 43
- 239000000203 mixture Substances 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 description 25
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 239000004988 Nematic liquid crystal Substances 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 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 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- REIVHYDACHXPNH-UHFFFAOYSA-N 2-fluoro-4-hydroxybenzonitrile Chemical compound OC1=CC=C(C#N)C(F)=C1 REIVHYDACHXPNH-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- LNEMDIUSUQPKIP-UHFFFAOYSA-N 2-phenyl-1,3-dioxane Chemical compound O1CCCOC1C1=CC=CC=C1 LNEMDIUSUQPKIP-UHFFFAOYSA-N 0.000 description 1
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
- GOUHYARYYWKXHS-UHFFFAOYSA-N 4-formylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=O)C=C1 GOUHYARYYWKXHS-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- -1 cyanophenyl ester Chemical class 0.000 description 1
- VJCWGXGMXAVKJU-UHFFFAOYSA-N cyclohexyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1CCCCC1 VJCWGXGMXAVKJU-UHFFFAOYSA-N 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- OPYYWWIJPHKUDZ-UHFFFAOYSA-N phenyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1=CC=CC=C1 OPYYWWIJPHKUDZ-UHFFFAOYSA-N 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6037884A JPS60204780A (ja) | 1984-03-28 | 1984-03-28 | ４−（トランス−５−アルキル−１，３−ジオキサ−２−イル）安息香酸誘導体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6037884A JPS60204780A (ja) | 1984-03-28 | 1984-03-28 | ４−（トランス−５−アルキル−１，３−ジオキサ−２−イル）安息香酸誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60204780A JPS60204780A (ja) | 1985-10-16 |
| JPS642595B2 true JPS642595B2 (en, 2012) | 1989-01-18 |
Family
ID=13140413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6037884A Granted JPS60204780A (ja) | 1984-03-28 | 1984-03-28 | ４−（トランス−５−アルキル−１，３−ジオキサ−２−イル）安息香酸誘導体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60204780A (en, 2012) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3405914A1 (de) * | 1984-02-18 | 1985-08-22 | Merck Patent Gmbh, 6100 Darmstadt | Fluessigkristalline verbindungen |
| JPS6178782A (ja) * | 1984-09-25 | 1986-04-22 | Dainippon Ink & Chem Inc | ３−フルオロ−４−シアノフエノ−ル誘導体 |
| JPH0825957B2 (ja) * | 1985-03-12 | 1996-03-13 | チッソ株式会社 | ジフルオロ芳香族化合物 |
-
1984
- 1984-03-28 JP JP6037884A patent/JPS60204780A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60204780A (ja) | 1985-10-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6144863B2 (en, 2012) | ||
| JPS642595B2 (en, 2012) | ||
| JPS59141527A (ja) | 部分還元されたナフタリン誘導体 | |
| JPH0142261B2 (en, 2012) | ||
| JP2897397B2 (ja) | ジフルオロベンゾニトリル誘導体及びそれを含有する液晶組成物及びそれを用いた液晶表示装置 | |
| JP2829436B2 (ja) | シクロブタン誘導体 | |
| 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 | |
| JP4094742B2 (ja) | エステル化合物ならびにそれを含有する液晶組成物 | |
| JPH05117206A (ja) | エステル化合物及びそれを含有する液晶組成物及びその液晶組成物を用いた液晶表示素子 | |
| JPH0629262B2 (ja) | ピリミジン誘導体 | |
| JPH0320378B2 (en, 2012) | ||
| JP4763943B2 (ja) | エステル化合物およびそれを含有する液晶組成物 | |
| JP2696963B2 (ja) | ピリミジン誘導体 | |
| JP2819645B2 (ja) | ピリミジン誘導体およびそれを含有する液晶組成物 | |
| JP2514395B2 (ja) | 側鎖にアルキル基を有する液晶性化合物 | |
| JPH0518821B2 (en, 2012) | ||
| JP2887693B2 (ja) | 小員環化合物 | |
| JP2822079B2 (ja) | シクロプロパン誘導体 | |
| JPH0142260B2 (en, 2012) | ||
| JP4023887B2 (ja) | エステル化合物およびそれを含有する液晶組成物 | |
| JPS60161941A (ja) | エ−テル結合を有するシクロヘキサン誘導体 | |
| JP2881994B2 (ja) | シクロヘキシルシクロヘキサン誘導体 | |
| JP2819682B2 (ja) | ピリミジン誘導体及び液晶組成物 | |
| JPS637169B2 (en, 2012) | ||
| JPS58148875A (ja) | ４−（トランス−５−アルキル−１，３−ジオキサ−２−イル）安息香酸エステル誘導体 |