394210-43-6

Basic information

• Product Name: 3-Oxazolidinecarboxylic acid, 2,5-dioxo-4-phenyl-, phenylmethyl ester
• CAS NO: 394210-43-6
• Molecular Formula: C17H13NO5
• Molecular Weight: 311.294
• Mol File: 394210-43-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Oxazolidinecarboxylic acid, 2,5-dioxo-4-phenyl-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Oxazolidinecarboxylic acid, 2,5-dioxo-4-phenyl-, phenylmethyl ester(394210-43-6)
• EPA Substance Registry System: 3-Oxazolidinecarboxylic acid, 2,5-dioxo-4-phenyl-, phenylmethyl ester(394210-43-6)

Safety Data

• Hazardous Substances Data: 394210-43-6(Hazardous Substances Data)

Upstream product

• 2835-06-5 phenylglycin 
• 5840-78-8 4-phenyl-oxazolidine-2,5-dione 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 17609-52-8 Z-D-phenylglycine 
• 64286-85-7 N-<(phenylmethoxy)carbonyl>-L-phenylalanine 2-propenyl ester 
• 470670-75-8 (R)-allyl-(N-benzyloxycarbonyl)phenylglycinate 
• 219323-43-0 (S)-ethyll 2-(benzyloxycarbonylamino)-2-phenylacetate 
• 5491-18-9 (S)-N-(benzyloxycarbonyl)phenylglycine 

Relevant articles and documents

Development of a rapid, room-temperature dynamic kinetic resolution for efficient asymmetric synthesis of α-aryl amino acids

equation presented A rapid, highly efficient and general dynamic kinetic resolution (DKR) of racemic α-aryl UNCAs with the dual-function catalysis of modified cinchona alkaloid was accomplished at room temperature. This DKR led to the development of a highly enantioselective catalytic method for the practical synthesis of a wide range of α-aryl and α-heteroaryl amino acids in 89-92% ee and 86-95% yield from racemic UNCAs.