130272-53-6

Basic information

• Product Name: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside
• Synonyms: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside
• CAS NO: 130272-53-6
• Molecular Weight: 248.279
• Mol File: 130272-53-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside(130272-53-6)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enoside(130272-53-6)

Safety Data

• Hazardous Substances Data: 130272-53-6(Hazardous Substances Data)

Upstream product

• 86470-08-8 methyl 4,6-O-benzylidene-β-D-galactopyranoside 3-O-p-toluenesulfonate 
• 2880-96-8 (1aR,2S,6R,7aR,7bR)-2-Methoxy-6-phenyl-hexahydro-1,3,5,7-tetraoxa-cyclopropa[a]naphthalene 
• 129263-16-7 methyl 2,3-bis-O-<(trifluoromethyl)sulfonyl>-4,6-O-(phenylmethylene)-β-D-galactopyranoside 
• 130187-36-9 methyl 2-O-benzenesulfonyl-4,6-O-benzylidene-3-O-p-toluenesulfonyl-β-D-galactoside 
• 130187-37-0 methyl 3-O-benzenesulfonyl-4,6-O-benzylidene-2-O-p-toluenesulfonyl-β-D-galactoside 
• 6748-86-3 methyl 4,6-O-benzylidene-β-D-galactopyranoside 2,3-di-O-p-toluenesulfonate 

Downstream Products

• 1185860-21-2 methyl-[O⁴,O⁶-((S)-benzylidene)-β-D-gulopyranoside] 
• 131985-36-9 methyl 4,6-di-O-benzyl-2,3-dideoxy-β-D-threo-hexoside 
• 132023-36-0 (4R,5R)-4,6-dibenzyloxy-5-p-toluenesulfonyloxyhexanal ethylene dithioacetal 
• 131985-39-2 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal ethylene dithioacetal 
• 131985-40-5 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal 
• 131985-37-0 (4R,5R)-4,6-dibenzyloxy-5-hydroxyhexanal ethylene dithioacetal 
• 132074-94-3 methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hexoside 

Relevant articles and documents

Synthesis of 3-azido-3-deoxy-β-d-galactopyranosides

Three efficient routes to 3-azido-3-deoxy-β-d-galactopyranosides were developed relying on a double inversion protocol at C3. Two of the routes were demonstrated to work with both O- and S-glycosides. In all three routes, the 2-O-acetyl-3-azido-4,6-O-benz

Free radical mediated reduction and deoxygenation of epoxides

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