177697-55-1

Basic information

• Product Name: (4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one
• Synonyms: (4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one
• CAS NO: 177697-55-1
• Molecular Weight: 295.338
• Mol File: 177697-55-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one(177697-55-1)
• EPA Substance Registry System: (4S)-4-phenyl-3-[(2R)-2-phenylpropionyl]oxazolidin-2-one(177697-55-1)

Safety Data

• Hazardous Substances Data: 177697-55-1(Hazardous Substances Data)

Upstream product

• 878194-06-0 (R)-pentafluorophenyl 2-phenylpropionate 
• 86217-38-1 4-phenyl-2-oxazolidinone 
• 99395-88-7 (S)-4-phenyl-2-oxazolidinone 
• 264621-69-4 ethyl (S)-2-oxooxazolidinine-4-carboxylate 
• 219951-25-4 (+/-)-pentafluorophenyl 2-phenylpropionate 
• 311310-18-6 (4S,2'R)-4-iso-propyl-3-(2'-phenylpropionyl)oxazolidin-2-one 
• 7782-26-5 (R)-2-Phenylpropionic acid 
• 186343-35-1 (S)-5-phenyl-1,3-oxazolidine-2-one 
• 25145-43-1 2-phenylpropionyl chloride 

Downstream Products

• 960210-90-6 1-phenylethyl 2-(6-methoxynaphthalen-2-yl)propionate 
• 79121-13-4 (R)-2-phenylpropionic acid-(R)-1-phenylethyl ester 
• 79121-15-6 (R,S)-Hydratropasaeure-1-phenylester 

Relevant articles and documents

Reaction of tributyltin hydride with α,β-unsaturated N-acyloxazolidinones

The treatment of tributyltin hydride with α-substituted propenoyl oxazolidinones in the presence of a catalytic amount of AIBN gave the tributyltin radical addition adduct when the substituent is an alkyl group. However, when the substituent is an aryl gr

Resolution of pentafluorophenyl 2-phenylpropanoate using combinations of quasi-enantiomeric oxazolidin-2-ones

The kinetic, mutual and parallel resolution of a series of structurally related active esters derived from 2-phenylpropanoic acid using a combination of quasi-enantiomeric oxazolidin-2-ones is discussed.

Parallel kinetic resolution of racemic oxazolidinones using quasi-enantiomeric active esters

Racemic Evans' oxazolidinones were efficiently resolved using a combination of quasi-enantiomeric profens. The levels of stereocontrol were high, leading to products with predictable configurations.