CAS 14233-48-8
:1,3,4,5-Tetra-O-benzyl-D-glucitol
Description:
1,3,4,5-Tetra-O-benzyl-D-glucitol is a chemical compound that belongs to the class of glucitol derivatives, specifically modified sugars. It features four benzyl groups attached to the hydroxyl positions of the D-glucitol molecule, which enhances its lipophilicity and alters its solubility properties compared to unmodified glucitol. This compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethanol, while being less soluble in water due to the bulky benzyl groups. The presence of these groups can also influence its reactivity and potential applications in organic synthesis, particularly in the field of carbohydrate chemistry. Additionally, 1,3,4,5-Tetra-O-benzyl-D-glucitol may serve as a protecting group in glycosylation reactions or as an intermediate in the synthesis of more complex carbohydrate structures. Its unique structural characteristics make it a valuable compound for research and development in various chemical applications.
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Found 3 products.
1,3,4,5-Tetra-O-benzyl-D-glucitol
CAS:Controlled ProductFormula:C34H38O6Color and Shape:NeatMolecular weight:542.662,3,4,6 -Tetra-O-benzyl-D-glucitol
CAS:<p>2,3,4,6 -Tetra-O-benzyl-D-glucitol is an atypical compound with a spectrum of activities. It has been shown to inhibit the synthesis of alditols and aldosides in vitro, and it also inhibits miglustat which is the first drug for Gaucher's disease approved by the FDA. 2,3,4,6 -Tetra-O-benzyl-D-glucitol is synthetically produced from D-glucose and benzyl chloride. The compound crystallizes as a chiral form that can exist as either (S) or (R) conformation. The (S) form has been observed to be more active than the (R) form against showdomycin and cyclic peptidase A.</p>Formula:C34H38O6Purity:Min. 95%Color and Shape:liquid.Molecular weight:542.66 g/mol
