403646-50-4

Basic information

• Product Name: S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside
• Synonyms: S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside
• CAS NO: 403646-50-4
• Molecular Weight: 600.733
• Mol File: 403646-50-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside(403646-50-4)
• EPA Substance Registry System: S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside(403646-50-4)

Safety Data

• Hazardous Substances Data: 403646-50-4(Hazardous Substances Data)

Upstream product

• 13992-16-0 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 108-98-5 thiophenol 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 824-94-2 p-methoxybenzyl chloride 
• 159407-19-9 phenyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside 

Downstream Products

• 1446474-51-6 2-azidoethyl 2,3-di-O-(p-methoxybenzyl)-4,6-O-benzylidene-β-D-mannopyranoside 
• 1450754-75-2 2-azidoethyl 2,3-di-O-(p-methoxybenzyl)-4,6-O-benzylidene-α-D-mannopyranoside 
• 1446474-52-7 phenyl (4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-β-D-mannopyranosyl)-(1→2)-4,6-O-benzylidene-3-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside 
• 1446474-57-2 2-azidoethyl (4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-β-D-mannopyranosyl)-(1→2)-4,6-O-benzylidene-3-O-(p-methoxybenzyl)-α-D-mannopyranoside 
• 1446474-53-8 2-azidoethyl (4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-β-D-mannopyranosyl)-(1→2)-4,6-O-benzylidene-3-O-(p-methoxybenzyl)-β-D-mannopyranoside 
• 407616-90-4 1-O-(4,6-O-benzylidene-2,3-di-O-dodecanoyl-β-D-mannopyranosyl)-3-O-tert-butyldimethylsilyl-2,4-O-ethylidene-D-erythritol 
• 407616-88-0 1-O-(4,6-O-benzylidene-2,3-di-O-p-methoxybenzyl-β-D-mannopyranosyl)-3-O-tert-butyldimethylsilyl-2,4-O-ethylidene-D-erythritol 
• 407616-89-1 1-O-(4,6-O-benzylidene-β-D-mannopyranosyl)-3-O-tert-butyldimethylsilyl-2,4-O-ethylidene-D-erythritol 
• 403646-68-4 4-(4-nitrophenyl)butyl 4,6-O-benzylidene-2-O-pivaloyl-3-O-[4-O-(4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-β-D-mannopyranosyl)-2,3-O-isopropylidene-α-L-rhamnopyranosyl]-β-D-galactopyranoside 
• 407616-85-7 (R_S)-S-phenyl 4,6-O-benzylidene-2,3-di-O-p-methoxybenzyl-1-thia-α-D-mannopyranoside S-oxide 

Relevant articles and documents

The composite body deproteinizing chitosanoligosaccharide-

Provided herein are conjugates comprising a protein and an oligosaccharide of one of Formulae I-VI. Also provided herein are pharmaceutical compositions comprising such conjugates. Further provided herein are methods of treating a lysosomal storage disorder in a mammal by administration of an oligosaccharide-glycoprotein conjugate.

Synthesis of the Salmonella type E(1) core trisaccharide as a probe for the generality of 1-(benzenesulfinyl)piperidine/triflic anhydride combination for glycosidic bond formation from thioglycosides.

A synthesis of a chromogenic glycoside of the Salmonella anatum group E(1) core trisaccharide is presented in which all three glycosidic bonds, a 1,2-cis-equatorial, a 1,2-trans-axial, and a 1,2-trans-equatorial linkage representing three of the four main classes of glycosidic bond, are formed with thioglycoside donors activated under a single set of conditions by the combination of 1-(benzenesulfinyl)piperidine and trifluoromethanesulfonic anhydride. 2,3-O-Carbonyl- and 2,3-O-isopropylidene-alpha-L-rhamnopyranosyl thioglycosides are found to be highly alpha-selective rhamnosyl donors under these conditions.