146137-35-1

Basic information

• Product Name: (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone
• Synonyms: (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone
• CAS NO: 146137-35-1
• Molecular Weight: 339.391
• Mol File: 146137-35-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone(146137-35-1)
• EPA Substance Registry System: (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone(146137-35-1)

Safety Data

• Hazardous Substances Data: 146137-35-1(Hazardous Substances Data)

Upstream product

• 20989-17-7 (2S)-2-phenylglycinol 
• 2935-35-5 (S)-2-phenylglycine 
• 99395-88-7 (S)-4-phenyl-2-oxazolidinone 
• 111292-75-2 (4S)-3-((2E)-2-butenoyl)-4-phenyl-1,3-oxazolidin-2-one 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 75-16-1 methylmagnesium bromide 
• 146137-31-7 (4S)-4-phenyl-3-<3-(4-methoxyphenyl)-2(E)-propenoyl>-2-oxazolidinone 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 151800-33-8 (3(2R,3S),4S)-3-<2-Azido-3-(4-methoxyphenyl)butyroyl>-4-phenyl-2-oxazolidinone 
• 151800-32-7 (3(3R),4R)-3-<3-(4'-Methoxyphenyl)butanoyl>-4-phenyl-2-oxazolidinone 
• 154006-51-6 (R)-3-((2R,3S)-2-bromo-3-(4-methoxyphenyl)butanoyl)-4-phenyloxazolidin-2-one 
• 128677-81-6 C₁₆H₂₂O₄ 
• 128677-84-9 (2R,3S)-2-Azido-3-(4-methoxyphenyl)butyric acid 
• 754977-47-4 (2R,3S)-2-Amino-3-(4-methoxy-phenyl)-butyric acid 
• 128573-11-5 threo-D-(2R,3S)-β-Methyltyrosine 
• 148706-34-7 (S)-3-[(2S,3S)-2-Bromo-3-(4-methoxy-phenyl)-butyryl]-4-phenyl-oxazolidin-2-one 
• 4974-05-4 (R)-(-)-4'-methoxy-3-phenylbutyric acid 

Relevant articles and documents

Asymmetric 1,4-Addition of Organocuprates to Chiral α,β-Unsaturated N-Acyl-4-phenyl-2-oxazolidinones: A New Approach to the Synthesis of Chiral β-Branched Carboxylic Acids

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Diastereospecific tandem Michael-like addition/electrophilic bromination: A one-pot tandem asymmetric synthesis of precursors of unusual amino acids

A systematic series of key intermediates of unusual β-methyl-amino acids have been synthesized by using a modified Evans auxiliary in an asymmetric Michael-like reaction followed by direct bromination in a one-pot reaction.