84207-46-5

3,4-Di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose Chemical Structure
84207-46-5

Chemical Structure

3,4-Di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose

  • CAS No.: 84207-46-5
  • Formula:C17H20O9S
  • Molecular Weight:400.40

IUPAC Name: (1R,2R,3S,4R,5R)-4-(tosyloxy)-6,8-dioxabicyclo[3.2.1]octane-2,3-diyl diacetate

InChIKey: JYMOPIWZWABELF-NQNKBUKLSA-N

SMILES: O=S(O[C@@H]1[C@H]([C@@H]([C@]2([H])O[C@@]1([H])OC2)OC(C)=O)OC(C)=O)(C3=CC=C(C=C3)C)=O

Biological Activity: 3,4-Di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose 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-W699077
3,4-Di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose 3,4-Di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose 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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