Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside is a glycoside derivative characterized by its unique structural features, which include a thioether linkage and a benzylidene acetal. This compound is derived from α-D-mannopyranose, a six-membered sugar ring, where the hydroxyl groups are modified to enhance stability and reactivity. The presence of the phenyl group contributes to its aromatic properties, while the benzylidene moiety provides steric hindrance and influences its solubility and reactivity in various chemical environments. The thioether functionality can impart distinct chemical reactivity, making it useful in synthetic organic chemistry, particularly in glycosylation reactions. Additionally, this compound may exhibit biological activity, potentially serving as a substrate or inhibitor in enzymatic processes involving glycosidases. Its specific applications and reactivity can vary based on the conditions under which it is used, including solvent choice and temperature. Overall, Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside is a valuable compound in both synthetic and medicinal chemistry contexts.

Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside

159407-19-9: Phenyl 4,6-O-(Phenylmethylene)-1-thio-a-D-mannopyranoside, Phenyl 4,6-O-[(R)-Phenylmethylene]-1-thio-a-D-mannopyranoside

Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside is a custom synthesis that is modified with fluorination, methylation and click modification. It is a monosaccharide that is used in the preparation of polysaccharides and glycosylations. Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside also has saccharide and carbohydrate properties.

CAS 159407-19-9: Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside

Phenyl 4,6-O-benzylidene-a-D-thiomannopyranoside

Ref: 3D-MP11291

Phenyl 4,6-O-benzylidene-1-thio-a-D-mannopyranoside

Ref: 7W-GC2057