β-D-Glucopyranose, 6-O-(triphenylmethyl)-, tetrabenzoate (CAS 85572-59-4) is a derivative of glucose that features a glucopyranose ring substituted at the 6-position with a triphenylmethyl group and tetrabenzoate moieties. This compound is characterized by its complex structure, which enhances its solubility and stability compared to its parent sugar. The presence of the triphenylmethyl group contributes to its hydrophobic properties, making it useful in various organic synthesis applications, particularly in protecting groups for hydroxyl functionalities. The tetrabenzoate groups further increase the molecular weight and can influence the compound's reactivity and interaction with other chemical species. This compound is typically used in research settings, particularly in carbohydrate chemistry and the development of glycosylation reactions. Its unique structural features allow for specific applications in drug delivery systems and materials science, where controlled release and stability are paramount. As with many organic compounds, proper handling and storage are essential to maintain its integrity and prevent degradation.

b-D-Glucopyranose,6-O-(triphenylmethyl)-, tetrabenzoate (9CI)

85572-59-4: β-D-Glucopyranose, 6-O-(triphenylmethyl)-, tetrabenzoate (CAS 85572-59-4) is a derivative of glucose that features a glucopyranose ring substituted at the 6-position with a triphenylmethyl group and tetrabenzoate moieties. This compound is characterized by its complex structure, which enhances its solubility and stability compared to its parent sugar. The presence of the triphenylmethyl group contributes to its hydrophobic properties, making it useful in various organic synthesis applications, particularly in protecting groups for hydroxyl functionalities. The tetrabenzoate groups further increase the molecular weight and can influence the compound's reactivity and interaction with other chemical species. This compound is typically used in research settings, particularly in carbohydrate chemistry and the development of glycosylation reactions. Its unique structural features allow for specific applications in drug delivery systems and materials science, where controlled release and stability are paramount. As with many organic compounds, proper handling and storage are essential to maintain its integrity and prevent degradation.

1,2,3,4-Tetra-O-benzoyl-6-O-trityl-b-D-glucopyranose

<p>1,2,3,4-Tetra-O-benzoyl-6-O-trityl-b-D-glucopyranose is a custom synthesis that can be used for methylation and Click modification. This compound is an oligosaccharide consisting of sugar molecules linked by glycosidic bonds. It is a polysaccharide with a saccharide repeating unit composed of monosaccharides. The carbohydrate chain contains 1,2,3,4 tetra O benzoyl groups and 6 O trityl groups. This product has a high purity and can be used in the synthesis of other compounds.<br>1,2,3,4 Tetra O benzoyl 6 O trityl b D glucopyranose (1) was synthesized from 4-(2'-hydroxyethyl)benzaldehyde (2), 4-(2'-hydroxyethyl)benzoic acid (3),</p>

CAS 85572-59-4

b-D-Glucopyranose,6-O-(triphenylmethyl)-, tetrabenzoate (9CI)

1,2,3,4-Tetra-O-benzoyl-6-O-trityl-b-D-glucopyranose

Ref: 7W-GC5866

1,2,3,4-Tetra-O-benzoyl-6-O-trityl-b-D-glucopyranose

Ref: 3D-MT08767