50605-09-9

2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose Chemical Structure
50605-09-9

Chemical Structure

2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose

  • CAS No.: 50605-09-9
  • Formula:C11H19NO6
  • Molecular Weight:261.27

IUPAC Name: N-((1R,2R)-1-hydroxy-1-((4S,5R)-5-hydroxy-2,2-dimethyl-1,3-dioxan-4-yl)-3-oxopropan-2-yl)acetamide

InChIKey: GIPVEPOQPWXJJC-SGIHWFKDSA-N

SMILES: CC(N[C@@H](C=O)[C@H]([C@@]1([H])[C@@H](COC(C)(O1)C)O)O)=O

Biological Activity: 2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose 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-W286946
2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose 2-(Acetylamino)-2-deoxy-4,6-O-(1-methylethylidene)-D-glucose 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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