161841-10-7

Basic information

• Product Name: C₁₇H₂₆O₄
• Synonyms: C₁₇H₂₆O₄
• CAS NO: 161841-10-7
• Molecular Weight: 294.391
• Mol File: 161841-10-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₇H₂₆O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₂₆O₄(161841-10-7)
• EPA Substance Registry System: C₁₇H₂₆O₄(161841-10-7)

Safety Data

• Hazardous Substances Data: 161841-10-7(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 53936-79-1 4-benzyloxyphenyl 2-tetrahydropyranyl ether 
• 103-16-2 4-Benzyloxyphenol 
• 2009-83-8 6-chloro-1-hexanol 
• 53936-56-4 4-(tetrahydro-2H-2-pyranyloxy)phenol 

Downstream Products

• 161841-11-8 C₂₀H₂₈O₅ 
• 161841-12-9 6-[(4-hydroxyphenyl)oxy]hexyl acrylate 

Relevant articles and documents

POLYMERIZABLE COMPOUND, COMPOSITION, POLYMER, OPTICALLY ANISOTROPIC BODY, LIQUID CRYSTAL DISPLAY ELEMENT, AND ORGANIC EL DEVICE

It is an object of the present invention to provide a polymerizable compound having a good liquid crystal property, a good alignment property, sufficient solubility in solvents, high preservation stability in a solution state, and high optical stability; a composition including the polymerizable compound; a polymer produced by polymerizing the polymerizable compound, such as a resin produced using the polymerizable compound; an optically anisotropic body including the polymer; and a liquid crystal display element and an organic EL device that include the optically anisotropic body. As a result of conducting intensive studies in order to achieve the above object, the compound represented by General Formula (I) is developed.

PROCESS FOR PREPARATION OF CYCLOALKANEDICARBOXYLIC ACID MONOESTERS

A process for preparation of cycloalkanedicarboxylic acid monoesters which is characterized by comprising: a first step of protecting two carboxyl groups (-COOH) of a compound represented by formula (1-A) with a group represented by Z to obtain a compound represented by formula (2-A), and a second step of deprotecting either of the groups represented by Z of the compound represented by formula (2-A) obtained in the first step with an acid to obtain a compound represented by formula (3-A). wherein m represents an integer of 0 to 3, p represents 0 or 1, Z represents a methylsulfanylmethyl group etc., and R5, R6 and R7 each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, a phenyl group or a benzyl group.