65827-58-9

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate Chemical Structure
65827-58-9

Chemical Structure

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate

  • CAS No.: 65827-58-9
  • Formula:C21H26O10
  • Molecular Weight:438.43

IUPAC Name: (2R,3S,4S,5R,6R)-6-(acetoxymethyl)-4-(benzyloxy)tetrahydro-2H-pyran-2,3,5-triyl triacetate

InChIKey: SJPSXDYBIIGRQJ-MJCUULBUSA-N

SMILES: O=C(OC[C@@H](O1)[C@@H](OC(C)=O)[C@H](OCC2=CC=CC=C2)[C@H](OC(C)=O)[C@H]1OC(C)=O)C

Biological Activity: α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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-W412469
α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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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