76926-67-5

Basic information

• Product Name: Carbamic acid, (1-phenylethyl)-, methyl ester
• CAS NO: 76926-67-5
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.219
• Mol File: 76926-67-5.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (1-phenylethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (1-phenylethyl)-, methyl ester(76926-67-5)
• EPA Substance Registry System: Carbamic acid, (1-phenylethyl)-, methyl ester(76926-67-5)

Safety Data

• Hazardous Substances Data: 76926-67-5(Hazardous Substances Data)

Upstream product

• 74-88-4 methyl iodide 
• 32366-25-9 1-azidoethylbenzene 
• 623-42-7 butanoic acid methyl ester 
• 618-36-0 rac-methylbenzylamine 
• 79-22-1 methyl chloroformate 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 67-56-1 methanol 
• 100-41-4 ethylbenzene 
• 598-55-0 methyl carbamate 
• 98-85-1 1-Phenylethanol 
• 1035813-57-0 C₁₁H₁₈NP 
• 98-86-2 acetophenone 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 67-56-1 methanol 
• 618-36-0 rac-methylbenzylamine 

Relevant articles and documents

Urethanes synthesis from oxamic acids under electrochemical conditions

Urethane synthesis via oxidative decarboxylation of oxamic acids under mild electrochemical conditions is reported. This simple phosgene-free route to urethanes involves an in situ generation of isocyanates by anodic oxidation of oxamic acids in an alcoholic medium. The reaction is applicable to a wide range of oxamic acids, including chiral ones, and alcohols furnishing the desired urethanes in a one-pot process without the use of a chemical oxidant.

Dynamic kinetic resolution of amines by using palladium nanoparticles confined inside the cages of amine-modified MIL-101 and lipase

Dynamic kinetic resolution (DKR) of amines is an important strategy for the synthesis of chiral drugs and their building blocks; however, improving the matchability of metal-catalyzed racemization and enzymatic resolution is still a task. In this paper, P

Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography

Efficient self-disproportionation of enantiomers of several non-racemic chiral amines was achieved through conversion to N-acetamides and subsequent MPLC using an achiral column. The MPLC of these non-racemic N-acetamide derivatives gave the chart having a clear boundary between two fractions. Thus, in the less polar fraction, remarkable enantiomer enrichment was observed (>99%ee), while the ee of more polar fraction was considerably reduced. The magnitude of the enantiomer enrichments and depletions strongly depended on substituent on the amino group.