JPH0256342B2 - - Google Patents
Info
- Publication number
- JPH0256342B2 JPH0256342B2 JP18376481A JP18376481A JPH0256342B2 JP H0256342 B2 JPH0256342 B2 JP H0256342B2 JP 18376481 A JP18376481 A JP 18376481A JP 18376481 A JP18376481 A JP 18376481A JP H0256342 B2 JPH0256342 B2 JP H0256342B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- compound
- bicyclohexylcarboxylate
- propyl
- 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
- 239000000126 substance Substances 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000001568 sexual effect Effects 0.000 claims 1
- 239000004973 liquid crystal related substance Substances 0.000 description 37
- 150000001875 compounds Chemical class 0.000 description 20
- 239000000203 mixture Substances 0.000 description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- -1 methoxymethylphenyl Chemical group 0.000 description 11
- AHXXIALEMINDAW-UHFFFAOYSA-N 4-(methoxymethyl)phenol Chemical compound COCC1=CC=C(O)C=C1 AHXXIALEMINDAW-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000000862 absorption spectrum Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 230000009102 absorption Effects 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 230000010287 polarization Effects 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- MKNQNPYGAQGARI-UHFFFAOYSA-N 4-(bromomethyl)phenol Chemical compound OC1=CC=C(CBr)C=C1 MKNQNPYGAQGARI-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BVJSUAQZOZWCKN-UHFFFAOYSA-N p-hydroxybenzyl alcohol Chemical compound OCC1=CC=C(O)C=C1 BVJSUAQZOZWCKN-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000001308 synthesis method Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QZMZUIGZTVFXKD-UHFFFAOYSA-N 1-ethoxy-4-(methoxymethyl)benzene Chemical compound CCOC1=CC=C(COC)C=C1 QZMZUIGZTVFXKD-UHFFFAOYSA-N 0.000 description 1
- HWMHRQOJZXBQBL-UHFFFAOYSA-N 4-(4-pentylcyclohexyl)cyclohexane-1-carbonitrile Chemical compound C1CC(CCCCC)CCC1C1CCC(C#N)CC1 HWMHRQOJZXBQBL-UHFFFAOYSA-N 0.000 description 1
- MTNZGYZWCQZBFV-UHFFFAOYSA-N 4-(4-propylcyclohexyl)cyclohexane-1-carbonyl chloride Chemical compound C1CC(CCC)CCC1C1CCC(C(Cl)=O)CC1 MTNZGYZWCQZBFV-UHFFFAOYSA-N 0.000 description 1
- JXPGQFKJNKWDKP-UHFFFAOYSA-N 4-(4-propylcyclohexyl)cyclohexane-1-carboxylic acid Chemical compound C1CC(CCC)CCC1C1CCC(C(O)=O)CC1 JXPGQFKJNKWDKP-UHFFFAOYSA-N 0.000 description 1
- XFMPTZWVMVMELB-UHFFFAOYSA-N 4-(4-propylphenyl)benzonitrile Chemical group C1=CC(CCC)=CC=C1C1=CC=C(C#N)C=C1 XFMPTZWVMVMELB-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001793 charged compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 125000004802 cyanophenyl group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18376481A JPS5885842A (ja) | 1981-11-18 | 1981-11-18 | 無色液晶性物質 |
| EP82101339A EP0058981B1 (en) | 1981-02-25 | 1982-02-22 | Colorless liquid crystalline compounds |
| DE8282101339T DE3268611D1 (en) | 1981-02-25 | 1982-02-22 | Colorless liquid crystalline compounds |
| US06/352,019 US4564694A (en) | 1981-02-25 | 1982-02-24 | Colorless liquid crystalline compounds |
| US06/761,885 US4694098A (en) | 1981-02-25 | 1985-08-02 | Colorless liquid crystalline compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18376481A JPS5885842A (ja) | 1981-11-18 | 1981-11-18 | 無色液晶性物質 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5885842A JPS5885842A (ja) | 1983-05-23 |
| JPH0256342B2 true JPH0256342B2 (en]) | 1990-11-29 |
Family
ID=16141556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18376481A Granted JPS5885842A (ja) | 1981-02-25 | 1981-11-18 | 無色液晶性物質 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5885842A (en]) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01104411U (en]) * | 1988-01-05 | 1989-07-14 |
-
1981
- 1981-11-18 JP JP18376481A patent/JPS5885842A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01104411U (en]) * | 1988-01-05 | 1989-07-14 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5885842A (ja) | 1983-05-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0253415B2 (en]) | ||
| JPH0613461B2 (ja) | フルオロフエニルシクロヘキサン誘導体 | |
| JPS6228137B2 (en]) | ||
| JPH0256342B2 (en]) | ||
| JPH0764829B2 (ja) | 液晶化合物 | |
| JP2789345B2 (ja) | 液晶性アルケニルエーテル化合物 | |
| JPH0825946B2 (ja) | フツ素置換ビフエニル誘導体 | |
| JP3226045B2 (ja) | フルオロトラン系アルケニル化合物 | |
| JP2884732B2 (ja) | フルオロトラン系化合物 | |
| JPS59167542A (ja) | 光学活性液晶 | |
| JP2528663B2 (ja) | 液晶性化合物 | |
| JP4115002B2 (ja) | 液晶化合物 | |
| JPH0680612A (ja) | 非光学活性液晶化合物 | |
| JP2854406B2 (ja) | βーケトカルボン酸誘導体 | |
| JP2534555B2 (ja) | 液晶性化合物及びそれを含む液晶組成物 | |
| JP2948897B2 (ja) | シクロヘキセン化合物および該化合物を含む液晶組成物 | |
| JPH0257533B2 (en]) | ||
| JP3432248B2 (ja) | シクロヘキセン誘導体 | |
| JP4039712B2 (ja) | 液晶組成物 | |
| JPH02178258A (ja) | ２―ハロゲン置換カルボン酸誘導体 | |
| JPH0588692B2 (en]) | ||
| JP2991454B2 (ja) | エーテル結合を有するシアノフェニルシクロヘキシルジオキサン | |
| JPS6067453A (ja) | ４−（４−アルコキシベンジリデンアミノ）ケイ皮酸エステル及びこれを含有する液晶 | |
| JPS6228136B2 (en]) | ||
| JPS61151187A (ja) | ２−（５−トランス−アルキル−１，３−ジオキサン−２−イル）−５−アルコキシピラジン |