28642-64-0

α-D-Glucopyranoside,methyl 4,6-O-(phenylmethylene),2-benzoate Chemical Structure
28642-64-0

Chemical Structure

α-D-Glucopyranoside,methyl 4,6-O-(phenylmethylene),2-benzoate

  • CAS No.: 28642-64-0
  • Formula:C21H22O7
  • Molecular Weight:386.40

IUPAC Name: (4aR,6S,7R,8S,8aS)-8-hydroxy-6-methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl benzoate

InChIKey: WHKUKOCUXSRSAR-QUJSNMKFSA-N

SMILES: O[C@H]1[C@@]2([H])[C@](COC(C3=CC=CC=C3)O2)([H])O[C@@H]([C@@H]1OC(C4=CC=CC=C4)=O)OC

Biological Activity: α-D-Glucopyranoside,methyl 4,6-O-(phenylmethylene),2-benzoate 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-W416041
α-D-Glucopyranoside,methyl 4,6-O-(phenylmethylene),2-benzoate α-D-Glucopyranoside,methyl 4,6-O-(phenylmethylene),2-benzoate 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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