16713-80-7

α-D-Glucofuranose,1,2:5,6-bis-O-(1-methylethylidene),3-acetate Chemical Structure
16713-80-7

Chemical Structure

α-D-Glucofuranose,1,2:5,6-bis-O-(1-methylethylidene),3-acetate

  • CAS No.: 16713-80-7
  • Formula:C14H22O7
  • Molecular Weight:302.32

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

InChIKey: QZKDRLZSJSWQPS-RMPHRYRLSA-N

SMILES: CC(O[C@H]1[C@]([C@]2([H])OC(C)(OC2)C)([H])O[C@@]3([H])[C@]1([H])OC(C)(O3)C)=O

Biological Activity: α-D-Glucofuranose,1,2:5,6-bis-O-(1-methylethylidene),3-acetate 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-W695196
α-D-Glucofuranose,1,2:5,6-bis-O-(1-methylethylidene),3-acetate α-D-Glucofuranose,1,2:5,6-bis-O-(1-methylethylidene),3-acetate 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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