93215-41-9

Phenylmethyl 2-(acetylamino)-2-deoxy-3-O-methyl-α-D-glucopyranoside Chemical Structure
93215-41-9

Chemical Structure

Phenylmethyl 2-(acetylamino)-2-deoxy-3-O-methyl-α-D-glucopyranoside

  • CAS No.: 93215-41-9
  • Formula:C16H23NO6
  • Molecular Weight:325.36

IUPAC Name: N-((2S,3R,4R,5S,6R)-2-(benzyloxy)-5-hydroxy-6-(hydroxymethyl)-4-methoxytetrahydro-2H-pyran-3-yl)acetamide

InChIKey: CQYQHQHAWKRHIV-QCODTGAPSA-N

SMILES: CC(N[C@H]1[C@H](O[C@@H]([C@H]([C@@H]1OC)O)CO)OCC2=CC=CC=C2)=O

Biological Activity: Phenylmethyl 2-(acetylamino)-2-deoxy-3-O-methyl-α-D-glucopyranoside 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-W416336
Phenylmethyl 2-(acetylamino)-2-deoxy-3-O-methyl-α-D-glucopyranoside Phenylmethyl 2-(acetylamino)-2-deoxy-3-O-methyl-α-D-glucopyranoside 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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