103674-69-7

α-D-Glucopyranuronic acid,1-bromo-1-deoxy,methyl ester,2,3,4-tribenzoate Chemical Structure
103674-69-7

Chemical Structure

α-D-Glucopyranuronic acid,1-bromo-1-deoxy,methyl ester,2,3,4-tribenzoate

  • CAS No.: 103674-69-7
  • Formula:C28H23BrO9
  • Molecular Weight:583.38

IUPAC Name: (2R,3R,4S,5S,6S)-2-bromo-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4,5-triyl tribenzoate

InChIKey: KXTNIKNREDJJSO-LKTXNROYSA-N

SMILES: O=C(C1=CC=CC=C1)O[C@H]2[C@@H]([C@H](O[C@@H]([C@@H]2OC(C3=CC=CC=C3)=O)Br)C(OC)=O)OC(C4=CC=CC=C4)=O

Biological Activity: α-D-Glucopyranuronic acid,1-bromo-1-deoxy,methyl ester,2,3,4-tribenzoate 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-W416162
α-D-Glucopyranuronic acid,1-bromo-1-deoxy,methyl ester,2,3,4-tribenzoate α-D-Glucopyranuronic acid,1-bromo-1-deoxy,methyl ester,2,3,4-tribenzoate 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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