183367-63-7

Basic information

• Product Name: 1-p-methylphenyltelluro-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside
• Synonyms: 1-p-methylphenyltelluro-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside
• CAS NO: 183367-63-7
• Molecular Weight: 798.316
• Mol File: 183367-63-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-p-methylphenyltelluro-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-p-methylphenyltelluro-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(183367-63-7)
• EPA Substance Registry System: 1-p-methylphenyltelluro-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(183367-63-7)

Safety Data

• Hazardous Substances Data: 183367-63-7(Hazardous Substances Data)

Upstream product

• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 32294-57-8 bis(4-methylphenyl)ditelluride 

Downstream Products

• 60045-26-3 3-phenylpropyl benzoate 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 114682-36-9 β-1-bromo-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside 
• 216006-43-8 phenyl 6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-(1→6)-2,3,4-tetra-O-benzoyl-β-D-glucopyranoside 
• 125135-28-6 methyl 6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 
• 32294-57-8 bis(4-methylphenyl)ditelluride 
• 10548-46-6 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose 
• 149818-84-8 methyl 6-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 
• 6899-46-3 2,3,4,6-tetra-O-benzoyl-1-O-cyclohexyl-β-D-glucopyranoside 

Relevant articles and documents

Reversible generation of glycosyl radicals from telluroglycosides under photochemical and thermal conditions

1-β-Telluroglycosides isomerize to α-isomers upon photolysis and thermolysis. The isomerization follows first-order reaction kinetics and proceeds through a glycosyl radical intermediate by homolytic C-Te bond cleavage. The radicals so generated are trapp

O-glycosidation of telluroglycoside by electrochemical oxidation

The electrochemical oxidation of telluroglycosides in the presence of primary or secondary alcohols results the O-glycosidation with high efficiency. Difference of the oxidation potential is nicely accounted for that of the reactivity of armed-and disarmed-telluroglycosides.