149206-46-2

Basic information

• Product Name: 3-OXAZOLIDINECARBOXYLIC ACID
• Synonyms: 3-OXAZOLIDINECARBOXYLIC ACID;5-OXO-4-(PHENYLMETHYL),1,1-DIMETHYLETHYL ESTER
• CAS NO: 149206-46-2
• Molecular Formula: C₁₅H₁₉NO₄
• Molecular Weight: 277.32
• Mol File: 149206-46-2.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-OXAZOLIDINECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-OXAZOLIDINECARBOXYLIC ACID(149206-46-2)
• EPA Substance Registry System: 3-OXAZOLIDINECARBOXYLIC ACID(149206-46-2)

Safety Data

• Hazardous Substances Data: 149206-46-2(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 75-11-6 diiodomethane 

Downstream Products

• 291279-17-9 N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine 
• 1356265-44-5 C₁₄H₁₆ClNO₄ 
• 34351-19-4 (3S)-3-amino-1-chloro-4-phenyl-2-butanone hydrochloride 
• 66605-57-0 (S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol 
• 37553-65-4 Boc-N-Me-Phe-OH 
• 103127-52-2 ((S)-1-benzylallyl)carbamic acid tert-butyl ester 

Relevant articles and documents

A novel synthesis of oxazolidin-5-one under basic condition

A simple and practical synthesis of oxazolidin-5-one is described under basic condition.

Process for Synthesizing Atazanavir

This invention relates to a process for synthesizing Atazanvir, including novel intermediates and novel steps to various intermediates along the synthetic pathway.

Stanna-Brook rearrangement of carboxylic acid derivatives. Synthetic utility and mechanistic studies

(Equation presented) The reaction of R3SnLi with carboxylic acid derivatives proceeds through a novel, very fast stanna-Brook rearrangement that generates α-alkoxyorganolithium compounds as intermediates. The outcome of these reactions depends on the nature of the carboxyl derivatives. Reaction of R3SnLi with ester derivatives gives rise to coupled products through a novel C-C bond formation reaction. Experimental evidence of the detailed reaction mechanism is provided.