68756-65-0

Basic information

• Product Name: cyclohexyl hydroxy(phenyl)acetate
• CAS NO: 68756-65-0
• Molecular Formula: C₁₄H₁₈O₃
• Molecular Weight: 234.2909
• Mol File: 68756-65-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 363.9°C at 760 mmHg
• Flash Point: 151.2°C
• Density: 1.14g/cm³
• Vapor Pressure: 6.19E-06mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: cyclohexyl hydroxy(phenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohexyl hydroxy(phenyl)acetate(68756-65-0)
• EPA Substance Registry System: cyclohexyl hydroxy(phenyl)acetate(68756-65-0)

Safety Data

• Hazardous Substances Data: 68756-65-0(Hazardous Substances Data)

Upstream product

• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 108-93-0 cyclohexanol 
• 611-73-4 Benzoylformic acid 
• 61598-01-4 phenylglyoxylic acid cyclohexyl ester 
• 1334313-44-8 (Z)-cyclohexyl 2-phenyl-2-(tosylhydrazono)acetate 
• 611-71-2 MANDELIC ACID 

Downstream Products

• 774-40-3 hydroxy-phenyl-acetic acid ethyl ester 
• 61598-01-4 phenylglyoxylic acid cyclohexyl ester 

Relevant articles and documents

Zirconocene-catalyzed direct (trans)esterification of acyl acids (esters) and alcohols in a strict 1:1 ratio under solvent-free conditions

A highly efficient way for the direct (trans)esterification of acyl acids (esters) and alcohols in a strict 1:1 ratio using a zirconocene complex (1, 1 mol%), a strong Lewis acid of good water tolerance, as a catalyst under solvent-free conditions has been developed. A wide range of acid and alcohol (esters) substrates undergo (trans)esterification to produce carboxylic ester motifs in moderate to good or excellent yields with good functional tolerance, such as that towards C-Br as well as CC and CC bonds. And complex 1 can be recycled six times without showing a significant decline in catalytic efficiency. It was demonstrated that cyclandelate, which is used to treat high blood pressure as well as heart and blood-vessel diseases, can be directly synthesized on a gram scale with 81% yield (6.70 g) using complex 1.

An efficient and convenient procedure for preparation of mandelates catalysed by TiO2/SO4/2- solid superacid

An easy and efficient synthesis of mandelates in excellent yields from mandelic acid with alcohols catalysed by TiO2/SO42- solid superacid.

A general and simple synthesis of phenylglyoxylic esters via the oxidation of mandelic esters with ammonium chlorochromate adsorbed on alumina

A general method for preparation of phenylglyoxylic esters by oxidation of mandelic esters with readily available ammonium chlorochromate adsorbed on alumina is described.