104013-04-9

3-Chloro-3-deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranose Chemical Structure
104013-04-9

Chemical Structure

3-Chloro-3-deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranose

  • CAS No.: 104013-04-9
  • Formula:C14H19ClO9
  • Molecular Weight:366.75

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

InChIKey: PVHZACAHYMQZEZ-DYPLGBCKSA-N

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

Biological Activity: 3-Chloro-3-deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranoseis 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].

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HY-W415975
3-Chloro-3-deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranose 3-Chloro-3-deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranoseis 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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