1615694-07-9

Basic information

• Product Name: (S)-3-(3-(2-chlorophenyl)propanoyl)-4-isopropyl-5,5-dimethyloxazolidin-2-one
• Synonyms: (S)-3-(3-(2-chlorophenyl)propanoyl)-4-isopropyl-5,5-dimethyloxazolidin-2-one
• CAS NO: 1615694-07-9
• Molecular Weight: 323.82
• Mol File: 1615694-07-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-3-(3-(2-chlorophenyl)propanoyl)-4-isopropyl-5,5-dimethyloxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-(3-(2-chlorophenyl)propanoyl)-4-isopropyl-5,5-dimethyloxazolidin-2-one(1615694-07-9)
• EPA Substance Registry System: (S)-3-(3-(2-chlorophenyl)propanoyl)-4-isopropyl-5,5-dimethyloxazolidin-2-one(1615694-07-9)

Safety Data

• Hazardous Substances Data: 1615694-07-9(Hazardous Substances Data)

Upstream product

• 52085-97-9 3-(2-chlorophenyl)propionyl chloride 
• 168297-86-7 (S)-4-isopropyl-5,5-dimethyloxazolidin-2-one 
• 1643-28-3 3-(2-chlorophenyl)propanoic acid 

Downstream Products

• 1615693-34-9 C₁₇H₂₁ClFNO₃ 

Relevant articles and documents

Stereoselective α-fluorination of N -acyloxazolidinones at room temperature within 1 h

A direct α-fluorination of N-acyloxazolidinones based on the unique reactivity of group IVa metal enolates has been developed. The reaction is an experimentally simple, low-cost, quick, and energy-efficient alternative for asymmetric α-fluorination of N-acyloxazolidinones. Preliminary studies have shown compatibility with alkyl, alkenyl, and alkynyl, aromatic, and several heteroaromatic substituents. High diastereoselectivities have been achieved with most substrates tested, and the reaction is typically complete within 1 h at ambient temperature.