6833-62-1

Basic information

• Product Name: trans-4-ethylcyclohexane carboxylic acid
• CAS NO: 6833-62-1
• Molecular Weight: 156.225
• Mol File: 6833-62-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: trans-4-ethylcyclohexane carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: trans-4-ethylcyclohexane carboxylic acid(6833-62-1)
• EPA Substance Registry System: trans-4-ethylcyclohexane carboxylic acid(6833-62-1)

Safety Data

• Hazardous Substances Data: 6833-62-1(Hazardous Substances Data)

Upstream product

• 619-64-7 p-ethylbenzoic acid 
• 622-96-8 4-methylethylbenzene 

Downstream Products

• 67589-87-1 4-Ethyl-cyclohexancarbonsaeurechlorid 
• 113296-33-6 (4-ethylcyclohexyl)methanol 
• 84856-09-7 Benzenesulfonic acid 2-(4-ethyl-cyclohexyl)-2-oxo-ethyl ester 
• 84855-64-1 2-Diazo-1-(4-ethyl-cyclohexyl)-ethanone 
• 92117-34-5 Toluene-4-sulfonic acid 2-(1,4-diethyl-cyclohexyl)-2-oxo-ethyl ester 
• 92117-32-3 Toluene-4-sulfonic acid 2-(1,4-diethyl-cyclohexyl)-2-oxo-ethyl ester 
• 92117-33-4 Benzenesulfonic acid 2-(1,4-diethyl-cyclohexyl)-2-oxo-ethyl ester 
• 92117-31-2 Benzenesulfonic acid 2-(1,4-diethyl-cyclohexyl)-2-oxo-ethyl ester 
• 92117-44-7 Benzenesulfonic acid 2-(4-ethyl-1-methyl-cyclohexyl)-2-oxo-ethyl ester 
• 92118-58-6 Benzenesulfonic acid 2-(4-ethyl-1-methyl-cyclohexyl)-2-oxo-ethyl ester 
• 114048-77-0 2-(cis-4-ethylcyclohexyl)-2-oxoethyl benzensulfonate 
• 114048-78-1 2-(trans-4-ethylcyclohexyl)-2-oxoethyl benzensulfonate 

Relevant articles and documents

Synthesis of Derivatives of 4-Ethylbenzoic and 4-Ethylcyclohexanecarboxylic Acids

A procedure has been developed for preparation of derivatives of 4-ethylbenzoic and 4-ethycyclohexanecarboxylic acids via liquid-phase catalytic oxidation and hydrogenation. From 4-ethylbenzoyl chloride the corresponding esters and N-arylamides have been synthesized, and from 4-ethylcyclohexanecarbonyl chloride, the corresponding N-arylamides.

Design, synthesis and structure-activity relationship studies of novel 4,4-bis(trifluoromethyl)imidazolines as acyl-CoA: Cholesterol acyltransferase (ACAT) inhibitors and antihypercholesterolemic agents

Novel 4,4-bis(trifluoromethyl)imidazolines have been found to be the potent acyl-CoA cholesterol acyltransferase (ACAT) inhibitors. ACAT is responsible for cholesterol esterification in the intestine, liver, and the arterial wall. These novel imidazolines

Studies on hypolipidemic agents. III. Synthesis and esterase-inhibitory activity of ω-cycloalkyl-2-oxoalkyl arenesulfonates

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