88073-02-3

Basic information

• Product Name: Carbamic acid, (2-oxo-2-phenylethoxy)-, ethyl ester
• Synonyms: ethyl phenacyloxycarbamate
• CAS NO: 88073-02-3
• Molecular Formula: C11H13NO4
• Molecular Weight: 223.229
• Mol File: 88073-02-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 81-82 °C
• Density: 1.180±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Carbamic acid, (2-oxo-2-phenylethoxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-oxo-2-phenylethoxy)-, ethyl ester(88073-02-3)
• EPA Substance Registry System: Carbamic acid, (2-oxo-2-phenylethoxy)-, ethyl ester(88073-02-3)

Safety Data

• Hazardous Substances Data: 88073-02-3(Hazardous Substances Data)

Upstream product

• 589-41-3 ethyl N-hydroxylcarbamate 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 41260-63-3 ethyl (2-phenyl-1-hydroxy-2-oxoethyl)carbamate 
• 38192-19-7 methyl 2-phenyl-1-hydroxy-2-oxoethylcarbamate 
• 88073-11-4 methyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate 
• 88073-10-3 ethyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate 

Relevant articles and documents

Reactivity of N-Phenacyloxycarbamates and Related Systems in the Presence of Bases: Study of a New Anionic Rearrangement

N-Phenacyloxycarbamates and other systems containing a CH2-O-N= framework, in the presence of bases, undergo a CH2-O-N= -> CH(OH)-N= rearrangement.The mechanism of this reaction has been studied kinetically and through crossover and capture experiments.The bulk of the data favours an intermolecular ionic mechanism which occurs by removal of a proton from the methylene group in the rate-determining step, followed by interaction between a glyoxal molecule and a carbamate anion in the fast step of the reaction.