1042065-80-4

Basic information

• Product Name: (2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine
• CAS NO: 1042065-80-4
• Molecular Weight: 311.378
• Mol File: 1042065-80-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine(1042065-80-4)
• EPA Substance Registry System: (2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine(1042065-80-4)

Safety Data

• Hazardous Substances Data: 1042065-80-4(Hazardous Substances Data)

Upstream product

• 6284-40-8 1-deoxy-1-(methylamino)-D-glucitol 
• 4748-78-1 4-ethylbenzylaldehyde 

Relevant articles and documents

An efficient and highly diastereoselective synthesis of C-glycosylated 1,3-oxazolidines from N-methyl-d-glucamine

A one-pot procedure for preparing chiral 1,3-oxazolidines derived from N-methyl-d-glucamine and aryl aldehydes is described. It has been carried out by using readily available reagents and operationally simple conditions allowing the preparation of the acyclic C-nucleoside analogs in high yields. The structure of these derivatives has been fully characterized by NMR correlations and single-crystal X-ray diffraction. Some reactions also provide access to the corresponding tetrahydro-1,3-oxazines by an alternative ring closure. Mechanistic considerations account for the observed steric course. Crown Copyright