6833-47-2

Basic information

• Product Name: trans-4-Ethylcyclohexanecarboxylic acid
• Synonyms: TRANS-4-ETHYLCYCLOHEXANECARBOXYLIC ACID;4-trans-ethyl-cyclohexane carboxylic acid;4-ETHYL HEXAHYDROBENZOIC ACID;Trans-4-EthylcyclohexaneCarboxylicacid,2HaC9H16O2;trans-4-Ethylhexahydrobenzoic acid;2HA;4-trans-ethylcyclohexyl carboxylic acid;trans-4-Ethylcyclohe
• CAS NO: 6833-47-2
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.22
• EINECS: 1312995-182-4
• Product Categories: Biphenyl & Diphenyl ether
• Mol File: 6833-47-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 48-51°C
• Boiling Point: 252.5 °C at 760 mmHg
• Flash Point: 120 °C
• Appearance: /
• Density: 0.999 g/cm³
• Vapor Pressure: 0.00602mmHg at 25°C
• Refractive Index: 1.463
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• PKA: 4.92±0.10(Predicted)
• CAS DataBase Reference: trans-4-Ethylcyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: trans-4-Ethylcyclohexanecarboxylic acid(6833-47-2)
• EPA Substance Registry System: trans-4-Ethylcyclohexanecarboxylic acid(6833-47-2)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-36-22
• Safety Statements: 26-36/37/39-37
• Hazardous Substances Data: 6833-47-2(Hazardous Substances Data)

Usage

Uses

Intermediates of Liquid Crystals

InChI:InChI=1/C9H16O2/c1-2-7-3-5-8(6-4-7)9(10)11/h7-8H,2-6H2,1H3,(H,10,11)/t7-,8-

Upstream product

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

Downstream Products

• 113296-33-6 (4-ethylcyclohexyl)methanol 

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

-