57783-81-0

Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-D-galactopyranoside Chemical Structure
57783-81-0

Chemical Structure

Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-D-galactopyranoside

  • CAS No.: 57783-81-0
  • Formula:C34H36O6
  • Molecular Weight:540.65

IUPAC Name: (2R,3S,4S,5R,6R)-4,5,6-tris(benzyloxy)-2-((benzyloxy)methyl)tetrahydro-2H-pyran-3-ol

InChIKey: HYZRJGYIUDQFSY-BWNLSPMZSA-N

SMILES: O[C@@H]([C@H](O[C@H]1OCC2=CC=CC=C2)COCC3=CC=CC=C3)[C@H](OCC4=CC=CC=C4)[C@H]1OCC5=CC=CC=C5

Biological Activity: Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-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-141413
Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-D-galactopyranoside Benzyl 2,3-Di-O-benzyl-4-O-benzoyl-β-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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