The chemical substance known as a-D-Glucopyranoside, methyl 4,6-O-[(4-methoxyphenyl)methylene]-2,3-bis-O-(phenylmethyl)-, with the CAS number 94902-60-0, is a complex glycoside derivative. It features a glucopyranoside backbone, which is a six-membered cyclic form of glucose, modified with multiple substituents that enhance its chemical properties. The presence of methoxy and phenylmethyl groups suggests that this compound may exhibit significant hydrophobic characteristics, potentially influencing its solubility and reactivity. The methylene bridge connecting the phenyl groups indicates a level of structural rigidity, which could affect its conformational dynamics. This compound may be of interest in various fields, including medicinal chemistry and biochemistry, due to its potential biological activities and applications in drug development. Its structural complexity also suggests that it could serve as a useful intermediate in organic synthesis or as a probe in biochemical studies. Overall, the unique combination of functional groups and structural features makes this compound a subject of interest for further research and exploration.

a-D-Glucopyranoside, methyl4,6-O-[(4-methoxyphenyl)methylene]-2,3-bis-O-(phenylmethyl)-

94902-60-0: The chemical substance known as a-D-Glucopyranoside, methyl 4,6-O-[(4-methoxyphenyl)methylene]-2,3-bis-O-(phenylmethyl)-, with the CAS number 94902-60-0, is a complex glycoside derivative. It features a glucopyranoside backbone, which is a six-membered cyclic form of glucose, modified with multiple substituents that enhance its chemical properties. The presence of methoxy and phenylmethyl groups suggests that this compound may exhibit significant hydrophobic characteristics, potentially influencing its solubility and reactivity. The methylene bridge connecting the phenyl groups indicates a level of structural rigidity, which could affect its conformational dynamics. This compound may be of interest in various fields, including medicinal chemistry and biochemistry, due to its potential biological activities and applications in drug development. Its structural complexity also suggests that it could serve as a useful intermediate in organic synthesis or as a probe in biochemical studies. Overall, the unique combination of functional groups and structural features makes this compound a subject of interest for further research and exploration.

Methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside

<p>Methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside is a monosaccharide that is used as a building block for the synthesis of complex carbohydrates. It has been modified with fluorination, methylation and glycosylation. Methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside can be synthesized using custom synthesis or high purity. This product has CAS No. 94902 60 0 and is available in high purity.</p>

CAS 94902-60-0

a-D-Glucopyranoside, methyl4,6-O-[(4-methoxyphenyl)methylene]-2,3-bis-O-(phenylmethyl)-

Methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside

Ref: 7W-GC0329

Methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside

Ref: 3D-MM08908