6748-91-0

Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside Chemical Structure
6748-91-0

Chemical Structure

Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside

  • CAS No.: 6748-91-0
  • Formula:C28H26O8
  • Molecular Weight:490.50

IUPAC Name: (4aR,6S,7R,8S,8aR)-6-methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-7,8-diyl dibenzoate

InChIKey: CGMUHSNJRXPSSA-IHTZYYJZSA-N

SMILES: O=C(C1=CC=CC=C1)O[C@H]2[C@@]3([H])[C@](COC(C4=CC=CC=C4)O3)([H])O[C@@H]([C@@H]2OC(C5=CC=CC=C5)=O)OC

Biological Activity: Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 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-W145615
Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 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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