141019-70-7

Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside Chemical Structure
141019-70-7

Chemical Structure

Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside

  • CAS No.: 141019-70-7
  • Formula:C29H29NO8
  • Molecular Weight:519.54

IUPAC Name: ((2R,3R,4R,5R,6S)-5-acetamido-4-(benzoyloxy)-6-(benzyloxy)-3-hydroxytetrahydro-2H-pyran-2-yl)methyl benzoate

InChIKey: MYVKGGKJMHXHHZ-KPTFLJRUSA-N

SMILES: CC(N[C@@H]1[C@H]([C@H]([C@H](O[C@@H]1OCC2=CC=CC=C2)COC(C3=CC=CC=C3)=O)O)OC(C4=CC=CC=C4)=O)=O

Biological Activity: Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside 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-W699261
Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-galactopyranoside 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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