JPS5675463A - Liquid crystal substance - Google Patents

Liquid crystal substance

Info

Publication number
JPS5675463A
JPS5675463A JP15176179A JP15176179A JPS5675463A JP S5675463 A JPS5675463 A JP S5675463A JP 15176179 A JP15176179 A JP 15176179A JP 15176179 A JP15176179 A JP 15176179A JP S5675463 A JPS5675463 A JP S5675463A
Authority
JP
Japan
Prior art keywords
formula
compound shown
liquid crystal
crystal substance
reacted
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
Application number
JP15176179A
Other languages
Japanese (ja)
Other versions
JPS6126978B2 (en
Inventor
Shigeru Sugimori
Hideo Sato
Kozo Hirata
Takashi Inukai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JNC Corp
Original Assignee
Chisso Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Chisso Corp filed Critical Chisso Corp
Priority to JP15176179A priority Critical patent/JPS5675463A/en
Publication of JPS5675463A publication Critical patent/JPS5675463A/en
Publication of JPS6126978B2 publication Critical patent/JPS6126978B2/ja
Granted legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

NEW MATERIAL:An alkoxyethoxyphenyl ester compound shown by the formula I (R1 and R2 are 1W10C alkyl).
EXAMPLE: Trans-4-propylcyclohexanecarboxylic acid-4-ethoxyphenyl ester.
USE: A liquid crystal compound. Having a negative dielectric anisotropy, and exhibiting a nematic temperature range of 28.2W42.2°C. Miscible with other liquid crystals, and effective for the improvement of a liquid crystal composition as a base, since this liquid crystal substance has a low viscosity at room temperature.
PROCESS: A compound shown by the formula II is reacted with a compound shown by the formula III, to give a compound shown by the formula IV, which is reacted with a compound shown by the formula V in the presence of pyridine, to give a compound shown by the formula I.
COPYRIGHT: (C)1981,JPO&Japio
JP15176179A 1979-11-22 1979-11-22 Liquid crystal substance Granted JPS5675463A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15176179A JPS5675463A (en) 1979-11-22 1979-11-22 Liquid crystal substance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15176179A JPS5675463A (en) 1979-11-22 1979-11-22 Liquid crystal substance

Publications (2)

Publication Number Publication Date
JPS5675463A true JPS5675463A (en) 1981-06-22
JPS6126978B2 JPS6126978B2 (en) 1986-06-23

Family

ID=15525711

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15176179A Granted JPS5675463A (en) 1979-11-22 1979-11-22 Liquid crystal substance

Country Status (1)

Country Link
JP (1) JPS5675463A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62129251A (en) * 1985-12-02 1987-06-11 Nippon Kayaku Co Ltd Trans-4-alkylcyclohexane-1-carboxylic acid ester

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62129251A (en) * 1985-12-02 1987-06-11 Nippon Kayaku Co Ltd Trans-4-alkylcyclohexane-1-carboxylic acid ester

Also Published As

Publication number Publication date
JPS6126978B2 (en) 1986-06-23

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