CAS 191036-43-8
:2,3-Di-O-benzyl-4-deoxy-L-fucose
Description:
2,3-Di-O-benzyl-4-deoxy-L-fucose is a synthetic derivative of fucose, a naturally occurring deoxy sugar. This compound features two benzyl groups attached to the 2 and 3 positions of the fucose molecule, enhancing its hydrophobic character and potentially influencing its biological interactions. The "4-deoxy" designation indicates the absence of a hydroxyl group at the 4-position, which can affect its reactivity and solubility. Typically, compounds like this are utilized in carbohydrate chemistry and glycosylation reactions, serving as intermediates in the synthesis of more complex oligosaccharides or glycoproteins. The presence of the benzyl groups can also provide protection for the hydroxyl groups during chemical transformations. In terms of physical properties, 2,3-Di-O-benzyl-4-deoxy-L-fucose is likely to be a white to off-white solid, soluble in organic solvents, and may exhibit specific optical activity due to its chiral nature. Its applications may extend to medicinal chemistry, particularly in the development of glycomimetics or in studies related to cell signaling and recognition processes.
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Found 3 products.
L-xylo-Hexose, 4,6-dideoxy-2,3-bis-O-(phenylmethyl)-
CAS:Formula:C20H24O4Color and Shape:LiquidMolecular weight:328.40222,3-Di-O-benzyl-4-deoxy-L-fucose
CAS:<p>2,3-Di-O-benzyl-4-deoxy--L-fucose is a methylated derivative of the fucose monosaccharide. It is synthesized through a click reaction that involves the use of an azide group on the sugar and an alkyne group on a thiol reagent. The synthesis utilizes one step, yielding 2,3-Di-O-benzyl-4-deoxy--L-fucose in high purity with low residual starting material. The product has been modified for glycosylation and can be used in oligosaccharides or polysaccharides.</p>Formula:C20H24O4Purity:Min. 95%Color and Shape:Clear Colourless LiquidMolecular weight:328.4 g/mol
