1429471-01-1

Basic information

• Product Name: benzyl (5S)-5-[(1S,2S)-1,2-dihydroxy-3-oxononyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate
• CAS NO: 1429471-01-1
• Molecular Weight: 407.507
• Mol File: 1429471-01-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl (5S)-5-[(1S,2S)-1,2-dihydroxy-3-oxononyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (5S)-5-[(1S,2S)-1,2-dihydroxy-3-oxononyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(1429471-01-1)
• EPA Substance Registry System: benzyl (5S)-5-[(1S,2S)-1,2-dihydroxy-3-oxononyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate(1429471-01-1)

Safety Data

• Hazardous Substances Data: 1429471-01-1(Hazardous Substances Data)

Upstream product

• 1155868-20-4 (S)-benzyl 5-(dihydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 7019-19-4 1-hydroxyoctan-2-one 
• 134038-74-7 benzyl (S)-5-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate 

Relevant articles and documents

Total synthesis of pipecolic acid and 1-: C -alkyl 1,5-iminopentitol derivatives by way of stereoselective aldol reactions from (S)-isoserinal

A short synthesis of iminosugars and pipecolic acid derivatives has been realized through aldol addition of a pyruvate, a range of ketones and (S)-isoserinal, followed by catalytic reductive intramolecular amination. The stereoselective aldol reaction was achieved successfully by using tertiary amines or di-zinc aldol catalysts, thus constituting two parallel routes to optically pure products with good yields and high diastereo-selectivities. These carbohydrate analogues may be the inhibitors of potent glycosidases and glycosyltransferases.