128677-90-7

Basic information

• Product Name: (4R)-3-(3'R)-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone
• Synonyms: (4R)-3-(3'R)-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone
• CAS NO: 128677-90-7
• Molecular Weight: 323.392
• Mol File: 128677-90-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4R)-3-(3'R)-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (4R)-3-(3'R)-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone(128677-90-7)
• EPA Substance Registry System: (4R)-3-(3'R)-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone(128677-90-7)

Safety Data

• Hazardous Substances Data: 128677-90-7(Hazardous Substances Data)

Upstream product

• 40217-17-2 (R)-4-(phenylmethyl)-2-oxazolidinone 
• 128677-86-1 C₁₅H₂₀O₃ 
• 772-14-5 (R)-3-phenylbutyric acid 
• 3282-30-2 pivaloyl chloride 
• 1517-69-7 (R)-1-phenylethanol 
• 666824-74-4 triethyl (2S)-2-phenylpropane-1,1,1-tricarboxylate 
• 4593-90-2 (S)-2-phenylbutanoic acid 
• 372504-89-7 (R)-4-benzyl-2-oxazolidinone lithium salt 

Downstream Products

• 128677-93-0 (2R)-azido-(3S)-phenylbutanoic acid 
• 59905-30-5 threo-D-(2R,3S)-β-methylphenylalanine 
• 128707-89-1 (4R)-3-(2'S,3'S)-2'-azido-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone 
• 128677-95-2 (2S,3S)-2-azido-3-phenylbutanoic acid 
• 25488-25-9 (2S,3S)-methylphenylalanine 
• 143251-56-3 (R)-4-Benzyl-3-((2S,3S)-2-bromo-3-phenyl-butyryl)-oxazolidin-2-one 
• 128707-87-9 (4S)-3-(2'R,3'S)-2'-azido-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone 

Relevant articles and documents

BETA-TETRAZOLYL-PROPIONIC ACIDS AS METALLO-BETA-LACTAMASE INHIBITORS

The present invention relates to compounds of formula I that are metallo-β-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with β-lactam antibiotics for overcoming resistance.

ASYMMETRIC SYNTHESIS OF UNUSUAL AMINO ACIDS: SYNTHESIS OF OPTICALLY PURE ISOMERS OF β-METHYLPHENYLALANINE

All the four individual isomers of β-methylphenylalanine have been synthesized in very high optical purities by utilizing in part the chiral imide enolate bromination methodology of Evans and co-workers.