79309-64-1

Basic information

• Product Name: ethoxy-(4-chloro-phenyl)-acetic acid ethyl ester
• CAS NO: 79309-64-1
• Molecular Weight: 242.702
• Mol File: 79309-64-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethoxy-(4-chloro-phenyl)-acetic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ethoxy-(4-chloro-phenyl)-acetic acid ethyl ester(79309-64-1)
• EPA Substance Registry System: ethoxy-(4-chloro-phenyl)-acetic acid ethyl ester(79309-64-1)

Safety Data

• Hazardous Substances Data: 79309-64-1(Hazardous Substances Data)

Upstream product

• 7138-34-3 p-chloromandelic acid 
• 75-03-6 ethyl iodide 
• 33512-03-7 3-(4-chlorophenyl)oxirane-2,2-dicarbonitrile 
• 64-17-5 ethanol 
• 14062-24-9 4-chloro-benzeneacetic acid, ethyl ester 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 141-52-6 sodium ethanolate 
• 2819-63-8 chloro-(4-chloro-phenyl)-acetic acid ethyl ester 

Relevant articles and documents

A facile one-pot synthesis of α-hydroxy acids and their derivatives

2-Substituted oxirane-1,1-dicarbonitriles react with water, alcohols or phenol to give 2-substituted 2-hydroxyacetic acids, alkyl-2-alkoxyacetates and phenyl 2-phenoxyacetates, respectively. Reaction of 2-substituted oxirane-1,1-dicarbonitrile with thiophenol and a nucleophile, typically water ethanol or urea, gave 2-(phenylthio)acetic acids, ethyl 2-(phenylthio)acetates and N-aminocarbonyl-2-(phenylthio)acetamides.

HYPERVALENT IODINE IN ORGANIC SYNTHESIS. A NEW ROUTE TO α-FUNCTIONALIZED CARBOXYLATE ESTERS.

Aryl and alkylcarboxylate esters are converted into the corresponding α-hydroxy acids or α-alkoxyesters upon treatment with C6H5I(OAc)2 and base in the appropriate solvent.