JPS59134767A - 負の誘電異方性を有するエステル化合物 - Google Patents

Info

Publication number

JPS59134767A

JPS59134767A JP889683A JP889683A JPS59134767A JP S59134767 A JPS59134767 A JP S59134767A JP 889683 A JP889683 A JP 889683A JP 889683 A JP889683 A JP 889683A JP S59134767 A JPS59134767 A JP S59134767A

Authority

JP

Japan

Prior art keywords

formula

liquid crystal

cyano

dielectric anisotropy

fluorophenol

Prior art date

1983-01-22

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

• Espacenet
• Global Dossier
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• -1 Ester compound Chemical class 0.000 title claims abstract description 8
• 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 26
• 125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
• 239000000203 mixture Substances 0.000 claims description 11
• 125000004432 carbon atom Chemical group C* 0.000 claims description 3
• 150000001875 compounds Chemical class 0.000 abstract description 16
• WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract description 12
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract description 6
• 239000000463 material Substances 0.000 abstract description 5
• MWLKQSIMPLORKX-UHFFFAOYSA-N 5-fluoro-2-hydroxybenzonitrile Chemical compound OC1=CC=C(F)C=C1C#N MWLKQSIMPLORKX-UHFFFAOYSA-N 0.000 abstract description 4
• 238000000034 method Methods 0.000 abstract description 3
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract description 3
• LSBFIKDJEJSBIJ-UHFFFAOYSA-N 4-fluoro-2-(hydroxyiminomethyl)phenol Chemical compound ON=CC1=CC(F)=CC=C1O LSBFIKDJEJSBIJ-UHFFFAOYSA-N 0.000 abstract description 2
• 239000000126 substance Substances 0.000 abstract description 2
• 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
• 239000013078 crystal Substances 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• 238000006243 chemical reaction Methods 0.000 description 3
• 238000004519 manufacturing process Methods 0.000 description 3
• LNEMDIUSUQPKIP-UHFFFAOYSA-N 2-phenyl-1,3-dioxane Chemical compound O1CCCOC1C1=CC=CC=C1 LNEMDIUSUQPKIP-UHFFFAOYSA-N 0.000 description 2
• BKZNEEWCEJKYMB-JOCQHMNTSA-N C1C[C@@H](CCC)CC[C@@H]1C(=O)OC1=CC=C(F)C=C1C#N Chemical compound C1C[C@@H](CCC)CC[C@@H]1C(=O)OC1=CC=C(F)C=C1C#N BKZNEEWCEJKYMB-JOCQHMNTSA-N 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• 239000004988 Nematic liquid crystal Substances 0.000 description 2
• 210000004027 cell Anatomy 0.000 description 2
• 210000002858 crystal cell Anatomy 0.000 description 2
• NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-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
• 150000002148 esters Chemical class 0.000 description 2
• 235000019441 ethanol Nutrition 0.000 description 2
• ZVQCKFRUFVAOTI-UHFFFAOYSA-N 1-propylcyclohexane-1-carbonyl chloride Chemical compound CCCC1(C(Cl)=O)CCCCC1 ZVQCKFRUFVAOTI-UHFFFAOYSA-N 0.000 description 1
• NMZPWKRKMBJEOZ-UHFFFAOYSA-N 4-propylcyclohexane-1-carbonyl chloride Chemical compound CCCC1CCC(C(Cl)=O)CC1 NMZPWKRKMBJEOZ-UHFFFAOYSA-N 0.000 description 1
• FDUBQNUDZOGOFE-UHFFFAOYSA-N 5-fluoro-2-hydroxybenzaldehyde Chemical compound OC1=CC=C(F)C=C1C=O FDUBQNUDZOGOFE-UHFFFAOYSA-N 0.000 description 1
• YGTOHJNZTCDYHV-HDJSIYSDSA-N C1C[C@@H](CCCC)CC[C@@H]1C(=O)OC1=CC=C(F)C=C1C#N Chemical compound C1C[C@@H](CCCC)CC[C@@H]1C(=O)OC1=CC=C(F)C=C1C#N YGTOHJNZTCDYHV-HDJSIYSDSA-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
• 239000002253 acid Substances 0.000 description 1
• 239000008186 active pharmaceutical agent Substances 0.000 description 1
• 235000010290 biphenyl Nutrition 0.000 description 1
• 239000004305 biphenyl Substances 0.000 description 1
• 239000000470 constituent Substances 0.000 description 1
• VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
• IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
• 230000003247 decreasing effect Effects 0.000 description 1
• 230000032050 esterification Effects 0.000 description 1
• 238000005886 esterification reaction Methods 0.000 description 1
• 238000003306 harvesting Methods 0.000 description 1
• 239000007788 liquid Substances 0.000 description 1
• 238000002844 melting Methods 0.000 description 1
• 230000008018 melting Effects 0.000 description 1
• 230000003287 optical effect Effects 0.000 description 1
• 150000002923 oximes Chemical class 0.000 description 1
• 238000007789 sealing Methods 0.000 description 1