220017-49-2

1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside Chemical Structure
220017-49-2

Chemical Structure

1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside

  • CAS No.: 220017-49-2
  • Formula:C26H44O10
  • Molecular Weight:516.62

IUPAC Name: (2R,3R,4S,5S)-5-((R)-1-hydroxy-2-(pivaloyloxy)ethyl)tetrahydrofuran-2,3,4-triyl tris(2,2-dimethylpropanoate)

InChIKey: QKVPHRSJRTWUAC-DISONHOPSA-N

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

Biological Activity: 1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside 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-W699949
1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside 1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside 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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