329365-81-3

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl methanethiosulfonate
• Synonyms: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl methanethiosulfonate
• CAS NO: 329365-81-3
• Molecular Weight: 634.815
• Mol File: 329365-81-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl methanethiosulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl methanethiosulfonate(329365-81-3)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl methanethiosulfonate(329365-81-3)

Safety Data

• Hazardous Substances Data: 329365-81-3(Hazardous Substances Data)

Upstream product

• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 1950-85-2 sodium methanethiosulfonate 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 2280-44-6 D-Glucose 

Downstream Products

• 1028451-00-4 phenyl-(2,3,4,6-tetra-O-benzyl-β-d-glucopyranosyl)disulfide 
• 77870-90-7 (S)-2-((benzyloxycarbonyl)amino)-3-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)propanoate 
• 77870-91-8 (S)-2-((benzyloxycarbonyl)amino)-3-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)propanoate 
• 41671-29-8 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranoside 
• 64842-82-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->6)-[1:2,3:4]-di-O-isopropylidene-α-D-galactopyranoside 
• 3879-79-6 methyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 19488-61-0 methyl 2,3,4,6-tetra-O-benzyl α-D-glucopyranoside 
• 329365-86-8 ethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl disulfide 

Relevant articles and documents

Glycosyl disulfides: Novel glycosylating reagents with flexible aglycon alteration

Glycosyl disulfides have been shown for the first time to be effective glycosyl donors. Glucosylation and galactosylation of a panel of representative alcohol acceptors allowed the formation of 28 simple glycosides, disaccharides, and glycoamino acids in yields of up to 90%. As well as providing a novel class of effective glycosyl donors, the ability to easily alter the nature of the aglycon and the ability to differently activate donors that differ only in their aglycon simply through altering conditions lends glycosyl disulfide donors to their use in latent-active reactivity tuning strategies.