67831-42-9

Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside Chemical Structure
67831-42-9

Chemical Structure

Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside

  • CAS No.: 67831-42-9
  • Formula:C34H36O6
  • Molecular Weight:540.65

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

InChIKey: HYZRJGYIUDQFSY-BGSSSCFASA-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: Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-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-W416106
Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-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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