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CAS 3082-95-9

:

methyl 2,3,4-tri-O-acetyl-D-glucopyranosiduronic acid

Description:
Methyl 2,3,4-tri-O-acetyl-D-glucopyranosiduronic acid is a derivative of glucuronic acid, characterized by the presence of three acetyl groups at the 2, 3, and 4 positions of the glucopyranose ring, along with a methyl ester at the carboxylic acid group. This compound is typically a white to off-white solid and is soluble in organic solvents such as methanol and dichloromethane, but may have limited solubility in water due to its hydrophobic acetyl groups. The acetylation enhances its stability and alters its reactivity, making it useful in various chemical syntheses and applications in biochemistry. It can serve as a building block for the synthesis of more complex carbohydrates or glycosides. The presence of the uronic acid moiety contributes to its potential biological activity, particularly in interactions with enzymes and receptors. As with many acetylated sugars, it may exhibit different physical and chemical properties compared to its non-acetylated counterparts, influencing its behavior in biological systems and chemical reactions.
Formula:C13H18O10
InChI:InChI=1/C13H18O10/c1-5(14)20-8-9(21-6(2)15)11(22-7(3)16)13(19-4)23-10(8)12(17)18/h8-11,13H,1-4H3,(H,17,18)/t8-,9-,10-,11+,13?/m0/s1
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