207396-23-4

Basic information

• Product Name: (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester
• Synonyms: (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester
• CAS NO: 207396-23-4
• Molecular Weight: 329.353
• Mol File: 207396-23-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester(207396-23-4)
• EPA Substance Registry System: (2R,3S)-N-benzyloxycarbonyl-3-phenylserine methyl ester(207396-23-4)

Safety Data

• Hazardous Substances Data: 207396-23-4(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 1262306-22-8 benzyloxycarbonylamino-4-chlorobenzoate 
• 103-26-4 Methyl cinnamate 
• 3426-71-9 Benzyl N-hydroxycarbamate 

Relevant articles and documents

Alkyl 4-chlorobenzoyloxycarbamates as highly effective nitrogen source reagents for the base-free, intermolecular aminohydroxylation reaction

Ethyl-(7), benzyl-(8), tert-butyl-(9), and fluorenylmethyl-4- chlorobenzoyloxycarbamates (10) have been prepared as storable and easy-to-prepare nitrogen sources for use in the intermolecular Sharpless aminohydroxylation reaction and its asymmetric variant. These reagents were found to be effective under base-free reaction conditions. The scope and limitations of these methods have been explored using a variety of alkenes, among which, trans-cinnamates, in particular, proved to be good substrates.