132074-94-3

Basic information

• Product Name: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hexoside
• CAS NO: 132074-94-3
• Molecular Weight: 250.295
• Mol File: 132074-94-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hexoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hexoside(132074-94-3)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hexoside(132074-94-3)

Safety Data

• Hazardous Substances Data: 132074-94-3(Hazardous Substances Data)

Upstream product

• 132074-89-6 methyl 4,6-O-benzylidene-2,3-dideoxy-α-D-threo-hex-2-enoside 
• 132074-90-9 methyl 4,6-O-benzylidene-2,3-di-O-[(methylthio)thiocarbonyl]-α-D-galactopyranoside 
• 64552-06-3 methyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 1373344-40-1 C₂₁H₂₂O₆S 
• 221662-13-1 methyl 2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside 
• 21193-75-9 D-galactal 
• 130272-53-6 methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside 
• 6748-86-3 methyl 4,6-O-benzylidene-β-D-galactopyranoside 2,3-di-O-p-toluenesulfonate 

Downstream Products

• 131985-37-0 (4R,5R)-4,6-dibenzyloxy-5-hydroxyhexanal ethylene dithioacetal 
• 131985-40-5 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal 
• 131985-38-1 2-mercaptoethyl 4,6-di-O-benzyl-1-thio-1,2,3-trideoxy-α-D-threo-hexoside 
• 131985-39-2 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal ethylene dithioacetal 
• 132023-36-0 (4R,5R)-4,6-dibenzyloxy-5-p-toluenesulfonyloxyhexanal ethylene dithioacetal 
• 131985-35-8 methyl 4,6-di-O-benzyl-2,3-dideoxy-α-D-threo-hexopyranoside 
• 131985-36-9 methyl 4,6-di-O-benzyl-2,3-dideoxy-β-D-threo-hexoside 

Relevant articles and documents

Bromodimethylsulfonium bromide catalyzed synthesis of methyl 2-dexoy-4,6-o-benzylidene galactopyranoside from galactal and the rapid route to 2,3- and 2,6-dideoxygalactopyranoses

4,6-O-Benzylidenation of D-galactal with PhCH(OCH3)2 catalyzed by bromodimethylsulfonium bromide leads to methyl 2-dexoy-4,6-O- benzylidene galactopyranoside efficiently, which serves as a key intermediate to the ready preparation of