210035-70-4

Basic information

• Product Name: 2,6-dimethylphenyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside
• Synonyms: 2,6-dimethylphenyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside
• CAS NO: 210035-70-4
• Molecular Weight: 410.488
• Mol File: 210035-70-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,6-dimethylphenyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dimethylphenyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside(210035-70-4)
• EPA Substance Registry System: 2,6-dimethylphenyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside(210035-70-4)

Safety Data

• Hazardous Substances Data: 210035-70-4(Hazardous Substances Data)

Upstream product

• 73-34-7 6-deoxy-L-galactose 
• 118-72-9 2,6-dimethylbenzene-1-thiol 
• 7404-35-5 1,2,3,4-tetra-O-acetyl-L-fucopyranose 
• 144-55-8 sodium hydrogencarbonate 

Downstream Products

• 210035-64-6 (2R,3S,4R,5R,6S)-3,4,5-Tris-benzyloxy-2-(2,6-dimethyl-benzenesulfinyl)-6-methyl-tetrahydro-pyran 
• 210035-71-5 2,6-dimethylphenyl 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside 
• 255047-50-8 2,6-dimethylphenyl 1-thio-β-L-fucopyranoside 

Relevant articles and documents

Sulfenate intermediates in the sulfoxide glycosylation reaction

The sulfoxide glycosylation reaction works remarkably well for many difficult glycosylations. We attribute this in part to the fact that an extremely reactive intermediate can be generated rapidly under mild conditions at low temperature. We find that ano

Glycosylation method

A method for forming a glycosidic linkage by: (a) contacting a glycoside bearing an anomeric sulfoxide group with a compound bearing a free hydroxyl group in the presence of an organic acid anhydride and a scavenger of sulfenyl esters; and (b) allowing a