JPH0414088B2 - - Google Patents
Info
- Publication number
- JPH0414088B2 JPH0414088B2 JP58240455A JP24045583A JPH0414088B2 JP H0414088 B2 JPH0414088 B2 JP H0414088B2 JP 58240455 A JP58240455 A JP 58240455A JP 24045583 A JP24045583 A JP 24045583A JP H0414088 B2 JPH0414088 B2 JP H0414088B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- trans
- formula
- ether
- 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 - Lifetime
Links
- 239000004973 liquid crystal related substance Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 description 16
- 239000004988 Nematic liquid crystal Substances 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- LOQLDQJTSMKBJU-UHFFFAOYSA-N 4-(chloromethyl)benzonitrile Chemical compound ClCC1=CC=C(C#N)C=C1 LOQLDQJTSMKBJU-UHFFFAOYSA-N 0.000 description 1
- VHWGPISIUNUREA-UHFFFAOYSA-N 4-pentylcyclohexan-1-ol Chemical compound CCCCCC1CCC(O)CC1 VHWGPISIUNUREA-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-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
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- WIJRMGQOERPOJA-UHFFFAOYSA-N benzyl cyanate Chemical compound N#COCC1=CC=CC=C1 WIJRMGQOERPOJA-UHFFFAOYSA-N 0.000 description 1
- 150000005524 benzylchlorides Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910052740 iodine Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000005699 methyleneoxy group Chemical group [H]C([H])([*:1])O[*:2] 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 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 |
|---|---|---|---|
| JP58240455A JPS60130542A (ja) | 1983-12-20 | 1983-12-20 | エ−テル結合を有する置換シクロヘキサン誘導体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58240455A JPS60130542A (ja) | 1983-12-20 | 1983-12-20 | エ−テル結合を有する置換シクロヘキサン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60130542A JPS60130542A (ja) | 1985-07-12 |
| JPH0414088B2 true JPH0414088B2 (fr) | 1992-03-11 |
Family
ID=17059748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58240455A Granted JPS60130542A (ja) | 1983-12-20 | 1983-12-20 | エ−テル結合を有する置換シクロヘキサン誘導体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60130542A (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010041419A1 (fr) | 2008-10-10 | 2010-04-15 | 東洋紡績株式会社 | Nouvelle protéine ayant une activité de fructosyl-valyl-histidine oxydase et produit modifié de celle-ci et utilisation de la protéine ou du produit modifié |
| US9260306B2 (en) | 2008-11-28 | 2016-02-16 | Kyoto University | Hydrogen fluoride purification method |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0315014B1 (fr) * | 1987-11-06 | 1994-01-12 | F. Hoffmann-La Roche Ag | Dérivés halogénés du benzène |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58121225A (ja) * | 1982-01-04 | 1983-07-19 | メルク・パテント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | ネマチツク相を有する異方性化合物及び該化合物を含有する液晶混合物 |
-
1983
- 1983-12-20 JP JP58240455A patent/JPS60130542A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58121225A (ja) * | 1982-01-04 | 1983-07-19 | メルク・パテント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | ネマチツク相を有する異方性化合物及び該化合物を含有する液晶混合物 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010041419A1 (fr) | 2008-10-10 | 2010-04-15 | 東洋紡績株式会社 | Nouvelle protéine ayant une activité de fructosyl-valyl-histidine oxydase et produit modifié de celle-ci et utilisation de la protéine ou du produit modifié |
| US9260306B2 (en) | 2008-11-28 | 2016-02-16 | Kyoto University | Hydrogen fluoride purification method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60130542A (ja) | 1985-07-12 |
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