Methyl 3-O-benzoyl-4,6-O-benzylidene-2-deoxyhexopyranoside, with the CAS number 32469-89-9, is a glycoside derivative characterized by its complex structure, which includes a methyl group, benzoyl group, and benzylidene moiety attached to a deoxyhexopyranose unit. This compound typically exhibits properties associated with both carbohydrates and aromatic compounds, such as solubility in organic solvents and potential reactivity due to the presence of functional groups. The benzoyl and benzylidene substituents contribute to its stability and may influence its reactivity in chemical reactions, particularly in glycosylation processes. Additionally, the presence of the deoxy sugar unit suggests that it may have biological relevance, potentially serving as a substrate or inhibitor in enzymatic reactions. Its structural features may also impart specific optical properties, making it of interest in studies involving chiral compounds. Overall, this compound is significant in the field of organic chemistry and may have applications in medicinal chemistry and the synthesis of more complex carbohydrate derivatives.

methyl 3-O-benzoyl-4,6-O-benzylidene-2-deoxyhexopyranoside

32469-89-9: Methyl 3-O-benzoyl-4,6-O-benzylidene-2-deoxyhexopyranoside, with the CAS number 32469-89-9, is a glycoside derivative characterized by its complex structure, which includes a methyl group, benzoyl group, and benzylidene moiety attached to a deoxyhexopyranose unit. This compound typically exhibits properties associated with both carbohydrates and aromatic compounds, such as solubility in organic solvents and potential reactivity due to the presence of functional groups. The benzoyl and benzylidene substituents contribute to its stability and may influence its reactivity in chemical reactions, particularly in glycosylation processes. Additionally, the presence of the deoxy sugar unit suggests that it may have biological relevance, potentially serving as a substrate or inhibitor in enzymatic reactions. Its structural features may also impart specific optical properties, making it of interest in studies involving chiral compounds. Overall, this compound is significant in the field of organic chemistry and may have applications in medicinal chemistry and the synthesis of more complex carbohydrate derivatives.

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CAS 32469-89-9

methyl 3-O-benzoyl-4,6-O-benzylidene-2-deoxyhexopyranoside

Methyl 2-deoxy-4,6-o-(phenylmethylene)-α-D-ribo-hexopyranoside benzoate

Ref: 3D-HBA46989