JPS5982382A - 含ハロゲンメタジオキサンエステル - Google Patents
含ハロゲンメタジオキサンエステルInfo
- Publication number
- JPS5982382A JPS5982382A JP19363982A JP19363982A JPS5982382A JP S5982382 A JPS5982382 A JP S5982382A JP 19363982 A JP19363982 A JP 19363982A JP 19363982 A JP19363982 A JP 19363982A JP S5982382 A JPS5982382 A JP S5982382A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- alkyl
- dioxan
- crystal compositions
- 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
- -1 M-dioxane ester Chemical class 0.000 title description 3
- 229910052736 halogen Inorganic materials 0.000 title 1
- 150000002367 halogens Chemical class 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 239000013078 crystal Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 150000007965 phenolic acids Chemical class 0.000 claims 1
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 26
- 239000000463 material Substances 0.000 abstract description 9
- 150000001875 compounds Chemical class 0.000 abstract description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 2
- GJGOEBMOOFMFHI-UHFFFAOYSA-N 4-(5-butyl-1,3-dioxan-2-yl)benzoic acid Chemical compound O1CC(CCCC)COC1C1=CC=C(C(O)=O)C=C1 GJGOEBMOOFMFHI-UHFFFAOYSA-N 0.000 abstract 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000000126 substance Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- LMYZQUNLYGJIHI-SPONXPENSA-N 4alpha-methyl-5alpha-cholest-7-en-3beta-ol Chemical compound C[C@@H]1[C@@H](O)CC[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@H](C)CCCC(C)C)CC[C@H]33)C)C3=CC[C@H]21 LMYZQUNLYGJIHI-SPONXPENSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LMYZQUNLYGJIHI-UHFFFAOYSA-N Methostenol Natural products CC1C(O)CCC2(C)C(CCC3(C(C(C)CCCC(C)C)CCC33)C)C3=CCC21 LMYZQUNLYGJIHI-UHFFFAOYSA-N 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 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 1
- XXUSEPRYHRDKFV-CTYIDZIISA-N C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C#N)C=C1 Chemical compound C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C#N)C=C1 XXUSEPRYHRDKFV-CTYIDZIISA-N 0.000 description 1
- YYAVXASAKUOZJJ-KOMQPUFPSA-N C1C[C@@H](CCCC)CC[C@@H]1C1=CC=C(C#N)C=C1 Chemical compound C1C[C@@H](CCCC)CC[C@@H]1C1=CC=C(C#N)C=C1 YYAVXASAKUOZJJ-KOMQPUFPSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 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 |
|---|---|---|---|
| JP19363982A JPS5982382A (ja) | 1982-11-04 | 1982-11-04 | 含ハロゲンメタジオキサンエステル |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19363982A JPS5982382A (ja) | 1982-11-04 | 1982-11-04 | 含ハロゲンメタジオキサンエステル |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5982382A true JPS5982382A (ja) | 1984-05-12 |
| JPH0318633B2 JPH0318633B2 (enrdf_load_html_response) | 1991-03-13 |
Family
ID=16311282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19363982A Granted JPS5982382A (ja) | 1982-11-04 | 1982-11-04 | 含ハロゲンメタジオキサンエステル |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5982382A (enrdf_load_html_response) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683078A (en) * | 1985-03-12 | 1987-07-28 | Chisso Corporation | Dihalogeno-aromatic compound |
| US4704227A (en) * | 1984-02-18 | 1987-11-03 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Liquid crystal compounds |
| US5230826A (en) * | 1987-11-06 | 1993-07-27 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| WO2013179960A1 (ja) * | 2012-05-28 | 2013-12-05 | Jnc株式会社 | 光学的に等方性の液晶媒体及び光素子 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55120580A (en) * | 1979-03-05 | 1980-09-17 | Timex Corp | Dioxanylphenylbenzoates |
| JPS57126486A (en) * | 1980-12-03 | 1982-08-06 | Timex Corp | 4-substituted phenyl-4'-(5-n-alkyl-1,3- dioxane-2-yl)benzoates |
| JPS57139074A (en) * | 1981-02-20 | 1982-08-27 | Chisso Corp | P-(trans-5-alkyl-1,3-dioxane-2-yl)phenyl p- halogenobenzoate |
-
1982
- 1982-11-04 JP JP19363982A patent/JPS5982382A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55120580A (en) * | 1979-03-05 | 1980-09-17 | Timex Corp | Dioxanylphenylbenzoates |
| JPS57126486A (en) * | 1980-12-03 | 1982-08-06 | Timex Corp | 4-substituted phenyl-4'-(5-n-alkyl-1,3- dioxane-2-yl)benzoates |
| JPS57139074A (en) * | 1981-02-20 | 1982-08-27 | Chisso Corp | P-(trans-5-alkyl-1,3-dioxane-2-yl)phenyl p- halogenobenzoate |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4704227A (en) * | 1984-02-18 | 1987-11-03 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Liquid crystal compounds |
| US4683078A (en) * | 1985-03-12 | 1987-07-28 | Chisso Corporation | Dihalogeno-aromatic compound |
| US4816179A (en) * | 1985-03-12 | 1989-03-28 | Chisso Corporation | Dihalogeno-aromatic compound |
| US5230826A (en) * | 1987-11-06 | 1993-07-27 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| US5302317A (en) * | 1987-11-06 | 1994-04-12 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| US5454974A (en) * | 1987-11-06 | 1995-10-03 | Hoffmann-La Roche Inc. | Halobenzene liquid crystals |
| WO2013179960A1 (ja) * | 2012-05-28 | 2013-12-05 | Jnc株式会社 | 光学的に等方性の液晶媒体及び光素子 |
| US9175222B2 (en) | 2012-05-28 | 2015-11-03 | Jnc Corporation | Optically isotropic liquid crystal medium and optical device |
| JPWO2013179960A1 (ja) * | 2012-05-28 | 2016-01-18 | Jnc株式会社 | 光学的に等方性の液晶媒体及び光素子 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0318633B2 (enrdf_load_html_response) | 1991-03-13 |
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