93474-58-9

Basic information

• Product Name: (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone
• Synonyms: (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone
• CAS NO: 93474-58-9
• Molecular Weight: 257.31
• Mol File: 93474-58-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone(93474-58-9)
• EPA Substance Registry System: (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone(93474-58-9)

Safety Data

• Hazardous Substances Data: 93474-58-9(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 93474-57-8 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid 

Downstream Products

• 93474-60-3 (3S,4S,5S)-N-(phenylsulfonyl)-4-amino-3,5-dihydroxy-3-methyl-1-hexene 

Relevant articles and documents

α-Amino Acids as Chiral Educts for Asymmetric Products. Chirospecific Syntheses of Methyl L-Sibirosaminide and Its C-3 Epimer from L-Allothreonine

Efficient syntheses of methyl L-sibirosaminide and its C-3 epimer are described using L-allothreonine as the chiral educt.Amino acylations of organometallics with the lithium salt of N-(phenylsulfonyl)-L-allothreonine constitute the key carbon-carbon bond