CAS 109581-83-1
:N-ACETYL-1-CHLORO-3,4,6-TRI-O-ACETYL-GALACTOSAMINIDE
Description:
N-Acetyl-1-chloro-3,4,6-tri-O-acetyl-galactosaminide is a synthetic carbohydrate derivative, specifically a modified form of galactosamine. This compound features an acetyl group at the nitrogen position, which enhances its solubility and stability. The presence of three acetyl groups on the hydroxyl positions (3, 4, and 6) of the galactosamine backbone contributes to its reactivity and potential applications in glycosylation reactions. The chlorine atom at the anomeric position (1) indicates that this compound can participate in nucleophilic substitution reactions, making it useful in organic synthesis and carbohydrate chemistry. Its structural modifications allow for increased lipophilicity and may influence its biological activity, potentially making it relevant in pharmaceutical research. The compound is typically handled with care due to the presence of reactive functional groups, and its applications may include studies in glycoprotein synthesis or as a building block in the development of glycomimetics.
Formula:C14H19ClNO9
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2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranosyl chloride
CAS:<p>2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranosyl chloride</p>Molecular weight:365.76349g/mol
