168397-51-1

2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl Chemical Structure
168397-51-1

Chemical Structure

2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl

  • CAS No.: 168397-51-1
  • Formula:C15H18N4O5
  • Molecular Weight:334.33

IUPAC Name: N-((2R,4aR,6R,7R,8R,8aS)-6-azido-8-hydroxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide

InChIKey: PEVZMZIOLKXJNJ-BXLXJSPXSA-N

SMILES: O[C@H]1[C@@]2([H])[C@](CO[C@@H](C3=CC=CC=C3)O2)([H])O[C@H]([C@@H]1NC(C)=O)N=[N+]=[N-]

Biological Activity: 2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].

Cat. No. Product Name Purity Description Pricing
HY-W145565
2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl 2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
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