CAS 174465-15-7
:4,6-Di-O-benzyliden-1,2,3-tri-O-pivaloyl-β-D-glucopyranose
Description:
4,6-Di-O-benzyliden-1,2,3-tri-O-pivaloyl-β-D-glucopyranose is a complex carbohydrate derivative characterized by its multiple protective groups, which enhance its stability and reactivity in synthetic applications. This compound features a glucopyranose backbone, which is a six-membered ring structure typical of glucose, modified with two benzylidene groups at the 4 and 6 positions and three pivaloyl groups at the 1, 2, and 3 positions. The presence of these bulky pivaloyl groups provides steric hindrance, which can influence the compound's reactivity and solubility. The benzylidene groups serve as protecting groups that can be removed under specific conditions, allowing for selective functionalization of the glucopyranose moiety. This compound is often utilized in carbohydrate chemistry for the synthesis of more complex glycosides or as an intermediate in the preparation of glycoproteins. Its unique structure and protective groups make it a valuable tool in organic synthesis, particularly in the development of carbohydrate-based pharmaceuticals and materials.
Formula:C28H40O9
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Found 2 products.
4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-glucopyranose
CAS:4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-glucopyranose is a carbohydrate that belongs to the group of saccharides. It is a simple sugar that has been modified with fluorination. This compound has been synthesized by custom synthesis and has high purity and can be used in research. 4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-glucopyranose is not currently available on the market.Formula:C28H40O9Purity:Min. 95%Molecular weight:520.63 g/mol
