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CAS 10227-17-5

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3,6-Di-O-acetyl-5-Deoxy-5-S-acetyl-1,2-O-isopropylidene-a-D-glucofuranose

Description:
3,6-Di-O-acetyl-5-deoxy-5-S-acetyl-1,2-O-isopropylidene-α-D-glucofuranose is a complex carbohydrate derivative characterized by its acetyl and isopropylidene functional groups. This compound features a furanose ring structure, which is a five-membered ring containing oxygen, derived from D-glucose. The presence of acetyl groups at the 3 and 6 positions enhances its stability and solubility in organic solvents, while the isopropylidene group at the 1 and 2 positions provides protection for the hydroxyl groups, making it less reactive. The 5-deoxy modification indicates the absence of a hydroxyl group at the 5 position, which can influence its biological activity and reactivity. This compound is typically used in organic synthesis and carbohydrate chemistry, particularly in the preparation of glycosides and other derivatives. Its unique structural features make it a valuable intermediate in the synthesis of more complex carbohydrates and potential pharmaceutical agents. As with many carbohydrate derivatives, it may exhibit specific stereochemical properties that are crucial for its reactivity and interactions in biological systems.
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