214492-02-1

Basic information

• Product Name: (4R)-3-((2S)-2-phenylpropionyl)-4-phenyl-oxazolidin-2-one
• Synonyms: (4R)-3-((2S)-2-phenylpropionyl)-4-phenyl-oxazolidin-2-one
• CAS NO: 214492-02-1
• Molecular Weight: 295.338
• Mol File: 214492-02-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4R)-3-((2S)-2-phenylpropionyl)-4-phenyl-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4R)-3-((2S)-2-phenylpropionyl)-4-phenyl-oxazolidin-2-one(214492-02-1)
• EPA Substance Registry System: (4R)-3-((2S)-2-phenylpropionyl)-4-phenyl-oxazolidin-2-one(214492-02-1)

Safety Data

• Hazardous Substances Data: 214492-02-1(Hazardous Substances Data)

Upstream product

• 90319-52-1 (4R)-phenyl-2-oxazolidinone 
• 17016-83-0 (4S)-4-isopropyl-1,3-oxazolidin-2-one 
• 219951-25-4 (+/-)-pentafluorophenyl 2-phenylpropionate 
• 878194-08-2 (4R,2'S)-3-[2'-(6-methoxy-naphthalen-2-yl)propionyl]-4-phenyl-oxazolidin-2-one 
• 7782-24-3 (S)-2-Phenylpropionic acid 
• 492-37-5 hydratropic acid 
• 54705-41-8 (5R)-5-phenyl-1,3-oxazolidin-2-one 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 931405-93-5 pentafluorophenyl (S)-2-phenylpropionate 
• 25145-43-1 2-phenylpropionyl chloride 

Downstream Products

• 54705-41-8 (5R)-5-phenyl-1,3-oxazolidin-2-one 
• 7782-24-3 (S)-2-Phenylpropionic acid 
• 198344-48-8 (4R,2'R)-3-(2'-phenylpropionyl)-4-phenyl-oxazolidin-2-one 
• 144789-14-0 allyl (S)-2-phenylpropanoate 
• 42253-99-6 ethyl (S)-2-phenylpropionate 
• 28645-07-0 (S)-methyl 2-phenylpropanoate 
• 90319-52-1 (4R)-phenyl-2-oxazolidinone 
• 37778-99-7 (S)-2-phenyl-1-propanol 

Relevant articles and documents

Efficient parallel resolution of an active ester of 2-phenylpropionic acid using quasi-enantiomeric Evans' oxazolidinones

The parallel kinetic resolution of pentafluorophenyl 2-phenylpropionate using an equimolar combination of quasi-enantiomeric oxazolidinones is discussed. The levels of diastereocontrol were excellent leading to separable quasi-enantiomeric syn-oxazolidino

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.