CAS 145852-76-2
:3,6-Di-O-benzyl-D-glucal
Description:
3,6-Di-O-benzyl-D-glucal is a chemical compound that belongs to the class of glucals, which are derivatives of glucose. This substance features two benzyl groups attached to the hydroxyl positions at the 3 and 6 positions of the glucal structure, enhancing its lipophilicity and potentially influencing its reactivity and solubility in organic solvents. The compound is characterized by its ability to participate in various chemical reactions, including glycosylation and other transformations typical of sugar derivatives. Its structure includes a double bond between the 1 and 2 carbon atoms, which is a defining feature of glucals, making it reactive in certain conditions. 3,6-Di-O-benzyl-D-glucal is often utilized in organic synthesis and carbohydrate chemistry, serving as an intermediate in the preparation of more complex glycosides and oligosaccharides. Additionally, due to its structural characteristics, it may exhibit biological activity, although specific biological properties would depend on the context of its use and the presence of other functional groups.
Formula:C20H22O4
InChI:InChI=1/C20H22O4/c21-20-18(24-14-17-9-5-2-6-10-17)11-12-23-19(20)15-22-13-16-7-3-1-4-8-16/h1-12,18-21H,13-15H2/t18-,19-,20+/m1/s1
Synonyms:- 1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol
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Found 3 products.
3,6-Di-O-benzyl-D-glucal
CAS:<p>3,6-Di-O-benzyl-D-glucal is a substrate for the enzyme fatty acid hydroxylase. This enzyme catalyzes the hydroxylation of fatty acids to produce hydroxy fatty acids and 3,6-di-O-benzyl-D-glucal. The stereoselective nature of this enzyme has been shown using microscopy to examine the reaction time in both monolayers and bilayers. The kinetics of this reaction have also been analyzed by kinetic analysis. It is thought that this reaction takes place in the cytosol, although it may also occur in mitochondria or chloroplasts.</p>Formula:C20H22O4Purity:Min. 95%Molecular weight:326.39 g/mol
