7772-79-4

β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate Chemical Structure
7772-79-4

Chemical Structure

β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate

  • CAS No.: 7772-79-4
  • Formula:C16H23NO10
  • Molecular Weight:389.35

IUPAC Name: (2S,3R,4R,5S,6R)-3-acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate

InChIKey: OVPIZHVSWNOZMN-OXGONZEZSA-N

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

Biological Activity: β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate 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-W009020
β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate 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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