CAS 81969-62-2
:a-D-Glucofuranose, 3,5,6-tris-O-(phenylmethyl)-
Description:
α-D-Glucofuranose, 3,5,6-tris-O-(phenylmethyl)-, with CAS number 81969-62-2, is a glycoside derivative of glucose characterized by the presence of three phenylmethyl (benzyl) groups attached to the hydroxyl positions at carbons 3, 5, and 6 of the furanose form of glucose. This compound exhibits a furanose ring structure, which is a five-membered cyclic form of glucose, contributing to its stability and reactivity. The phenylmethyl substituents enhance the lipophilicity of the molecule, potentially affecting its solubility and interaction with biological systems. The presence of these substituents can also influence the compound's reactivity in various chemical reactions, making it useful in synthetic organic chemistry and potentially in medicinal chemistry for drug development. Additionally, the compound may exhibit specific stereochemical properties due to the configuration of the anomeric carbon and the orientation of the substituents, which can be crucial for its biological activity and interactions.
Formula:C27H30O6
Synonyms:- 3,5,6-Tri-O-benzyl-a-D-glucofuranose
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Found 3 products.
3,5,6-Tri-O-benzyl-D-glucofuranose
CAS:3,5,6-Tri-O-benzyl-D-glucofuranose is a crystalline and white or off-white powder. It is soluble in water and toluene, but insoluble in chlorinated solvents. The chemical has been synthesized from benzoic acid and D-glucose. 3,5,6-Tri-O-benzyl-D-glucofuranose is used as a reagent for the synthesis of polyhydroxybutyrate (PHB) polymers that are biodegradable and can be used as thermoplastic polyesters. This compound has been shown to be potentially hazardous to the environment due to its high reactivity with chloride ions in the presence of benzyl alcohols.Formula:C27H30O6Purity:Min. 95%Molecular weight:450.54 g/mol
