250607-11-5

Basic information

• Product Name: 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one
• Synonyms: 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one
• CAS NO: 250607-11-5
• Molecular Weight: 247.294
• Mol File: 250607-11-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one(250607-11-5)
• EPA Substance Registry System: 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one(250607-11-5)

Safety Data

• Hazardous Substances Data: 250607-11-5(Hazardous Substances Data)

Upstream product

• 183059-24-7 tert-butyl (2-hydroxy-2-methylpropyl)carbamate 
• 250607-20-6 3-(1'-hydroxy-2'-benzylpropyl)-5,5-dimethyloxazolidin-2-one 
• 223906-54-5 N-(2-Methyl-1-oxo-3-phenylpropyl)-5,5-dimethyloxazolidin-2-one 
• 1121-83-1 5,5-dimethyl-oxazolidin-2-one 
• 645-45-4 hydrocinnamic acid chloride 

Downstream Products

• 88842-13-1 (Z-)-ethyl 5-phenylpent-2-enoate 
• 55282-95-6 ethyl (2E)-5-phenylpent-2-enoate 
• 250607-19-3 3-(2'-benzylpent-4'-enoyl)-5,5-dimethyloxazolidin-2-one 
• 1121-83-1 5,5-dimethyl-oxazolidin-2-one 
• 27829-72-7 ethyl (E)-hex-2-enoate 
• 27829-71-6 (Z)-ethyl hex-2-enoate 
• 104-53-0 3-phenyl-propionaldehyde 
• 608138-16-5 3-(1'-hydroxy-2'-benzylpent-4'-enyl)-5,5-dimethyloxazolidin-2-one 
• 250607-20-6 3-(1'-hydroxy-2'-benzylpropyl)-5,5-dimethyloxazolidin-2-one 

Relevant articles and documents

Enantioselective Protonation of Cyclic Carbonyl Ylides by Chiral Lewis Acid Assisted Alcohols

Chiral Lewis acid-catalyzed asymmetric alcohol addition reactions to cyclic carbonyl ylides generated from N-(α-diazocarbonyl)-2-oxazolidinones featuring a dual catalytic system are reported. Construction of a chiral quaternary heteroatom-substituted carb

N-acyl-5,5-dimethyl-oxazolidin-2-ones as latent aldehyde equivalents

N-acyl-5,5-dimethyl-oxazolidin-2-ones can function as versatile latent aldehyde equivalents - reductive cleavage with DIBAL-H affords aldehydes in good yield, while tandem DIBAL-H/Wittig methodology affords α,β-unsaturated esters.