2774-29-0

3-Deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-xylo-hexofuranose Chemical Structure
2774-29-0

Chemical Structure

3-Deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-xylo-hexofuranose

  • CAS No.: 2774-29-0
  • Formula:C12H20O5
  • Molecular Weight:244.28

IUPAC Name: (3aR,5R,6aR)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole

InChIKey: AKKRBVFGAWFTRW-ZYUZMQFOSA-N

SMILES: CC1(O[C@@](CO1)([H])[C@@]2([H])C[C@]3([H])[C@](OC(C)(O3)C)([H])O2)C

Biological Activity: 3-Deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-xylo-hexofuranose 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-W404399
3-Deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-xylo-hexofuranose 3-Deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-xylo-hexofuranose 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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