133125-16-3

Basic information

• Product Name: (2S,4R)-3-Benzoyl-2-tert-butyl-4-methyl-4-phenyl-oxazolidin-5-one
• CAS NO: 133125-16-3
• Molecular Weight: 337.419
• Mol File: 133125-16-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,4R)-3-Benzoyl-2-tert-butyl-4-methyl-4-phenyl-oxazolidin-5-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R)-3-Benzoyl-2-tert-butyl-4-methyl-4-phenyl-oxazolidin-5-one(133125-16-3)
• EPA Substance Registry System: (2S,4R)-3-Benzoyl-2-tert-butyl-4-methyl-4-phenyl-oxazolidin-5-one(133125-16-3)

Safety Data

• Hazardous Substances Data: 133125-16-3(Hazardous Substances Data)

Upstream product

• 630-19-3 pivalaldehyde 
• 98-88-4 benzoyl chloride 
• 104057-63-8 Sodium; (S)-2-[2,2-dimethyl-prop-(E)-ylideneamino]-propionate 
• 104057-64-9 (2S,4S)-3-benzoyl-2-(tert-butyl)-4-methyl-1,3-oxazolidin-5-one 

Downstream Products

• 29738-09-8 (R)-2-amino-2-phenylpropanoic acid 

Relevant articles and documents

Synthese enantioselective d'α-aryl amino acides: subtitution nucleophile aromatique sur le fluorobenzene chrome tricarbonyle d'enolates chiraux

We report here a convenient synthesis of optically pure α-aryl amino acids by enantioselective substitution of fluorobenzene tricarbonylchromium using the Schiff bases of L-alanine methyl ester with (1R,2R,5R)-2-hydroxy-3-pinanone in presence of LDA or deprotonated 2-(tert-butyl)-4-methyl-1,3-oxazolidin-5 one.