113304-18-0

Basic information

• Product Name: 5-Oxazolidinone, 3-benzoyl-2-(1,1-dimethylethyl)-4-methylene-, (S)-
• CAS NO: 113304-18-0
• Molecular Formula: C15H17NO3
• Molecular Weight: 259.305
• Mol File: 113304-18-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-Oxazolidinone, 3-benzoyl-2-(1,1-dimethylethyl)-4-methylene-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Oxazolidinone, 3-benzoyl-2-(1,1-dimethylethyl)-4-methylene-, (S)-(113304-18-0)
• EPA Substance Registry System: 5-Oxazolidinone, 3-benzoyl-2-(1,1-dimethylethyl)-4-methylene-, (S)-(113304-18-0)

Safety Data

• Hazardous Substances Data: 113304-18-0(Hazardous Substances Data)

Upstream product

• 630-19-3 pivalaldehyde 
• 98-88-4 benzoyl chloride 
• 147092-24-8 (2S,4S)-3-benzoyl-2-t-butyl-4-<(methylsulfonyl)methyl>oxazolidin-5-one 
• 104057-64-9 (2S,4S)-3-benzoyl-2-(tert-butyl)-4-methyl-1,3-oxazolidin-5-one 

Downstream Products

• 207796-10-9 (2S,5R,6R,8R)-1-Benzoyl-2-tert-butyl-8-isobutyl-4-oxo-6-phenyl-3-oxa-1,7-diaza-spiro[4.4]nonane-8-carboxylic acid methyl ester 

Relevant articles and documents

Asymmetric Synthesis of Chiral Cyclic Amino Acids by Diels-Alder Reactions of (2S)- and (2R)-4-Methyleneoxazolidin-5-ones

The synthesis of chiral (2S)- and (2R)-4-methyleneoxazolidin-5-ones, in high enantiomeric purity from (S)-S-methylcysteine, and their highly exo-selective Diels-Alder reactions with cyclic dienes are described. (1R,2S,4S)-2-Aminobicycloheptane-2-ca

A Convenient Method for the Synthesis of β-substituted α-Amino Acids. Diastereoselective Conjugate Addition of Nitronates to a Chiral Dehydroalanine Derivative

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104. Bromination of Cyclic Acetals from α-Amino Acids and α- or β-Hydroxy Acids with N-Bromosuccinimide

The preparation of novel electrophylic building blocks for the synthesis of enantiomerically pure compounds (EPC) is described.Thus, the 2-(tert-butyl)dioxolanones, -oxazolidinones, -imidazolidinones, and -dioxanones obtained by acetalization of pivalalde