13639-54-8

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate Chemical Structure
13639-54-8

Chemical Structure

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate

  • CAS No.: 13639-54-8
  • Formula:C17H24O10S2
  • Molecular Weight:452.50

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

InChIKey: GYORARISFGRNMU-LJIZCISZSA-N

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

Biological Activity: 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate 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-W700094
2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate 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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