76352-71-1

Basic information

• Product Name: Benzenepropanoic acid, a-ethyl-, methyl ester
• CAS NO: 76352-71-1
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 76352-71-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, a-ethyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, a-ethyl-, methyl ester(76352-71-1)
• EPA Substance Registry System: Benzenepropanoic acid, a-ethyl-, methyl ester(76352-71-1)

Safety Data

• Hazardous Substances Data: 76352-71-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 56640-46-1 1-(phenylmethyl)butanoic acid 
• 4379-25-3 ethyl-benzyl-malonic acid 
• 100-44-7 benzyl chloride 
• 100-52-7 benzaldehyde 
• 76154-00-2 diethyl ester of benzylethylmalonic acid 
• 620-79-1 Ethyl 2-benzylacetoacetate 
• 108975-05-9 ethyl α-ethyl-α-benzylacetoacetate 
• 186581-53-3 diazomethane 
• 620-78-0 ethyl 3-phenylpropenoic acid 

Downstream Products

• 175698-03-0 methyl 2-(cyanomethyl)-2-(phenylmethyl)butanoate 
• 111654-30-9 2-Benzyl-butyric acid 3-phenoxy-benzyl ester 

Relevant articles and documents

NEW METHOD FOR GENERATION OF THIOCARBONYL YLIDES FROM BIS(TRIMETHYLSILYLMETHYL)SULFOXIDES AND THEIR APPLICATION TO CYCLOADDITIONS

Thiocarbonyl ylides were generated by heating of bis(trimethylsilylmethyl)sulfoxides.Cycloadditions of the ylides in the presence of dipolarophiles proceeded smoothly to give di- or tetrahydrothiophenes.

Synthesis of 3-Phenoxybenzyl 3-Alkyl-3-phenyl-/p-substituted phenyl and 3-Phenoxybenzyl 2-Alkyl-3-phenyl-/p-substituted phenylpropionates

Some 3-phenoxybenzyl 3-alkyl-3-phenyl-/p-substituted phenylpropionates (VII, XI, XV, XIX, XXIII, XXVII) which resemble structurally the 1,2-secopyrethroids, have been prepared employing simple reactions like alkylation, decarbethoxylation and transesterification.The synthesis of 3-phenoxybenzyl 2-alkyl-3-phenyl-/p-substituted phenyl-propionates (XXXI, XXXII, XXXIII, and XXXVI) bearing close structural resemblance to 2,3-secopyrethroids has also been described.