29776-43-0

2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-D-glucopyranose Chemical Structure
29776-43-0

Chemical Structure

2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-D-glucopyranose

  • CAS No.: 29776-43-0
  • Formula:C15H19NO6
  • Molecular Weight:309.31

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

InChIKey: OIXDAEIOQFFRMF-SNNRFPGISA-N

SMILES: O[C@H]1[C@@]2([H])[C@](COC(C3=CC=CC=C3)O2)([H])OC([C@@H]1NC(C)=O)O

Biological Activity: 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-D-glucopyranose 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-W353732
2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-D-glucopyranose 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-D-glucopyranose 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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