115439-41-3

Basic information

• Product Name: (S)-3-[2-(2-Benzyloxy-phenyl)-acetyl]-4-isopropyl-oxazolidin-2-one
• CAS NO: 115439-41-3
• Molecular Weight: 353.418
• Mol File: 115439-41-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-3-[2-(2-Benzyloxy-phenyl)-acetyl]-4-isopropyl-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-[2-(2-Benzyloxy-phenyl)-acetyl]-4-isopropyl-oxazolidin-2-one(115439-41-3)
• EPA Substance Registry System: (S)-3-[2-(2-Benzyloxy-phenyl)-acetyl]-4-isopropyl-oxazolidin-2-one(115439-41-3)

Safety Data

• Hazardous Substances Data: 115439-41-3(Hazardous Substances Data)

Upstream product

• 17016-83-0 (4S)-4-isopropyl-1,3-oxazolidin-2-one 
• 115439-34-4 (2-benzyloxy-phenyl)-acetyl chloride 

Downstream Products

• 115439-43-5 (S)-3-[(2S,3S)-3-(4-Benzyloxy-phenyl)-2-(2-benzyloxy-phenyl)-3-hydroxy-propionyl]-4-isopropyl-oxazolidin-2-one 

Relevant articles and documents

Stereoselective Synthesis of the Dihydrobenzofuran Segments of the Ephedradine Alkaloids

Syntheses of dihydrobenzofuran derivatives have involved formation of phenol substituted β-hydroxy esters by an aldol reaction followed by Lewis-acid-catalysed intramolecular cyclisation as key steps; the use of chiral oxazolidinones in the aldol reaction has formed the basis of enantiospecific syntheses.