152870-51-4

Basic information

• Product Name: methyl 4-S-benzoyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside
• Synonyms: methyl 4-S-benzoyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside
• CAS NO: 152870-51-4
• Molecular Weight: 282.361
• Mol File: 152870-51-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 4-S-benzoyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-S-benzoyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside(152870-51-4)
• EPA Substance Registry System: methyl 4-S-benzoyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside(152870-51-4)

Safety Data

• Hazardous Substances Data: 152870-51-4(Hazardous Substances Data)

Upstream product

• 152870-48-9 methyl 3-O-tertbutyldimethylsilyl-2,6-dideoxy-α-D-lyxo-pyranoside 
• 198011-32-4 methyl 2-deoxy-α,β-glycoside 
• 134355-03-6 6-deoxy-D-glucal 
• 28170-13-0 thiobenzoic acid potassium salt 
• 98-91-9 thiobenzoic acid 
• 152870-50-3 methyl 4-S-benzoyl-3-O-tertbutyldimethylsilyl-2,6-dideoxy-4-thio-α-D-arabino-hexopyranoside 

Downstream Products

• 330450-36-7 Methyl 4-(3-O,4-S-dibenzoyl-2,6-dideoxy-4-thio-β-D-ribo-hexopyranosyloxyamino)-4,6-dideoxy-2-O-{4'-[N-ethyl-N-(fluoren-9-ylmethoxycarbonyl)amino]butyl}-α-D-glucopyranoside 
• 330450-30-1 3-O,4-S-Dibenzoyl-2,6-dideoxy-4-thio-D-ribo-hexopyranosyl trichloroacetimidate 
• 219702-30-4 Methyl 3-O,4-S-dibenzoyl-2,6-dideoxy-4-thio-α-D-ribo-hexopyranoside 
• 152844-41-2 methyl 3-O-benzoyl-2,6-dideoxy-4-thio-α-D-ribo-hexopyranoside 
• 219702-29-1 Methyl 4-S-benzoyl-2,6-dideoxy-4-thio-3-O-(2,2,2-trifluoroethylsulfonyl)-α-D-arabino-hexopyranoside 

Relevant articles and documents

Synthesis of 2,6-Dideoxy-4-S-Methyl-4-Thio-D-ribo-Hexopyranose, A Component of the Esperamicin Oligosaccharide

Two synthetic approaches to 2,6-dideoxy-4-S-methyl-4-thio-D-ribo pyranose, a component of the oligosaccharide of esperamicins are described.An asymmetric synthesis, starting from the propargylic alcohol dimer, relies on the Sharpless asymmetric epoxidation and the regioselective opening of epoxy alcohols.The other synthesis is based on stereocontrolled transformations of a readily available sugar precursor, D-galactose.