157896-05-4

Basic information

• Product Name: Phenyl 2,3,4,6-tetra-O-benzoyl-1-seleno-β-D-glucopyranoside
• Synonyms: Phenyl 2,3,4,6-tetra-O-benzoyl-1-seleno-β-D-glucopyranoside
• CAS NO: 157896-05-4
• Molecular Weight: 735.649
• Mol File: 157896-05-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenyl 2,3,4,6-tetra-O-benzoyl-1-seleno-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl 2,3,4,6-tetra-O-benzoyl-1-seleno-β-D-glucopyranoside(157896-05-4)
• EPA Substance Registry System: Phenyl 2,3,4,6-tetra-O-benzoyl-1-seleno-β-D-glucopyranoside(157896-05-4)

Safety Data

• Hazardous Substances Data: 157896-05-4(Hazardous Substances Data)

Upstream product

• 4981-97-9 phenyl 1-seleno-β-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 23661-29-2 phenyl 2,3,4,6-tetra-O-acetyl-1-seleno-β-D-glucopyranoside 
• 14262-85-2 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl iodide 
• 1666-13-3 diphenyl diselenide 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 

Downstream Products

• 139903-49-4 phenyl 2,3,4,6-tetra-O-benzyl-1-seleno-β-D-glycopyranoside 
• 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 
• 14262-85-2 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl iodide 
• 4981-97-9 phenyl 1-seleno-β-D-glucopyranoside 
• 70751-54-1 1,2:3:4-di-O-isopropylidene-6-O-(tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-galactose 

Relevant articles and documents

Selective activation of glycosyl donors utilising electrochemical techniques: A study of the thermodynamic oxidation potentials of a range of chalcoglycosides

A series of six chalcoglycosides (phenyl-2,3,4,6-tetra-0-benzoyl-1-seleno-β-D-glucopyranoside, phenyl-2,3,4,6-tetraO-benzyl-1-seleno-β-D-glucopyranoside, phenyl-2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside, p-tolyl-2,3,4,6-O-benzoyl-1-thio-β-D-glucop

The synthesis of some selenoand telluro-β-d-glucopyranosides

Several new seleno- and telluro-β-D-glucopyranosides have been prepared by treatment of protected α-D-glucopyranosyl bromides with the appropriate dialkyl or diaryl dichalcogenide and sodium borohydride in ethanol.