4515-24-6

2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine Chemical Structure
4515-24-6

Chemical Structure

2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine

  • CAS No.: 4515-24-6
  • Formula:C14H22N2O8
  • Molecular Weight:346.33

IUPAC Name: (2R,3S,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate

InChIKey: DKGKXBJJPLBTOQ-DHGKCCLASA-N

SMILES: CC(O[C@H]1[C@@H]([C@H](O[C@H]([C@@H]1NC(C)=O)N)COC(C)=O)OC(C)=O)=O

Biological Activity: 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine 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-W357136
2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine 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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