188893-00-7

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl 2'-pyridyl sulfone
• Synonyms: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl 2'-pyridyl sulfone
• CAS NO: 188893-00-7
• Molecular Weight: 665.807
• Mol File: 188893-00-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl 2'-pyridyl sulfone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl 2'-pyridyl sulfone(188893-00-7)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl 2'-pyridyl sulfone(188893-00-7)

Safety Data

• Hazardous Substances Data: 188893-00-7(Hazardous Substances Data)

Upstream product

• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl trichloroacetimidate 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 136984-91-3 2-pyridyl 2,3,4,6-tetra-O-benzyl-1-thio-α-D-mannopyranoside 

Downstream Products

• 1351076-62-4 methyl 3-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)propanoate 
• 251456-69-6 methyl 6-O-acetyl-2,4-di-O-benzyl-3-deoxy-3-C-(1'-(2',3',4',6'-tetra-O-benzyl-1'-deoxy-α-D-mannopyranosyl)(oxythiocarbonylimidazolyl)methyl)-α-D-mannopyranoside 
• 251456-75-4 Imidazole-1-carbothioic acid O-[((1R,2S,3S,4S,5R)-2,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-yl)-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl] ester 
• 251456-71-0 Acetic acid (2R,3S,4S,5S,6S)-3,5-bis-benzyloxy-6-methoxy-4-((2R,3R,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-ylmethyl)-tetrahydro-pyran-2-ylmethyl ester 
• 503456-89-1 methyl 2,3,6-tri-O-benzyl-4-deoxy-4-C-[(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)(hydroxy)methyl]-α-D-mannopyranoside 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 177696-56-9 1,5-anhydro-2,3,4,6-tetra-O-benzyl-α-D-manno-hexitol 

Relevant articles and documents

A general approach to 1,2-trans-C-glycosides via glycosyl samarium(III) compounds

The samarium diiodide reduction of glycosyl pyridyl sulfones with ketones or aldehydes under Barbier conditions leads to the instantaneous and stereospecific formation of 1,2trans-C-glycosides in good to acceptable yields. Mannosyl pyridyl sulfones 5ac,h