α-D-Mannopyranoside, methyl 4,6-O-(phenylmethylene)-, diacetate (CAS 6748-84-1) is a glycoside derivative of mannose, characterized by its pyranose ring structure. This compound features a methoxy group at the anomeric carbon, along with two acetyl groups and a phenylmethylene protecting group on the 4 and 6 hydroxyl positions. The presence of these functional groups contributes to its solubility in organic solvents and its reactivity in various chemical transformations. It is typically used in synthetic organic chemistry, particularly in the synthesis of more complex carbohydrates or as an intermediate in the preparation of glycosylated compounds. The diacetate form indicates that the hydroxyl groups are protected, which can facilitate selective reactions. Additionally, this compound may exhibit specific stereochemical properties due to the configuration of the mannose unit, influencing its biological activity and interactions. Overall, α-D-Mannopyranoside derivatives are valuable in research and industrial applications, particularly in the fields of biochemistry and pharmaceuticals.

a-D-Mannopyranoside, methyl4,6-O-(phenylmethylene)-, diacetate (9CI)

6748-84-1: α-D-Mannopyranoside, methyl 4,6-O-(phenylmethylene)-, diacetate (CAS 6748-84-1) is a glycoside derivative of mannose, characterized by its pyranose ring structure. This compound features a methoxy group at the anomeric carbon, along with two acetyl groups and a phenylmethylene protecting group on the 4 and 6 hydroxyl positions. The presence of these functional groups contributes to its solubility in organic solvents and its reactivity in various chemical transformations. It is typically used in synthetic organic chemistry, particularly in the synthesis of more complex carbohydrates or as an intermediate in the preparation of glycosylated compounds. The diacetate form indicates that the hydroxyl groups are protected, which can facilitate selective reactions. Additionally, this compound may exhibit specific stereochemical properties due to the configuration of the mannose unit, influencing its biological activity and interactions. Overall, α-D-Mannopyranoside derivatives are valuable in research and industrial applications, particularly in the fields of biochemistry and pharmaceuticals.

Methyl 2,3-di-O-acetyl-4,6-O-benzylidene-a-D-mannopyranoside

<p>Methyl 2,3-di-O-acetyl-4,6-O-benzylidene-a-D-mannopyranoside is a synthetic compound that has not been studied in vivo or in vitro. Methyl 2,3-di-O-acetyl-4,6-O-benzylidene-aDmannopyranoside is an oligosaccharide that can be modified with fluorination and methylation. It is synthesized by glycosylation of a Dmannopyranose using an acetate as the acyl donor. The acetate is then selectively benzylated to form the desired product.</p>

CAS 6748-84-1

a-D-Mannopyranoside, methyl4,6-O-(phenylmethylene)-, diacetate (9CI)

Methyl 2,3-di-O-acetyl-4,6-O-benzylidene-a-D-mannopyranoside

Ref: 7W-GC5721

Methyl 2,3-di-O-acetyl-4,6-O-benzylidene-a-D-mannopyranoside

Ref: 3D-MM08892