132063-03-7

2-Acetamido-4,6-O-benzylidene-2-deoxy-D-gluconohydroximo-1,5-lactone Chemical Structure
132063-03-7

Chemical Structure

2-Acetamido-4,6-O-benzylidene-2-deoxy-D-gluconohydroximo-1,5-lactone

  • CAS No.: 132063-03-7
  • Formula:C15H18N2O6
  • Molecular Weight:322.31

IUPAC Name: N-((2R,4aR,7R,8R,8aS,E)-8-hydroxy-6-(hydroxyimino)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide

InChIKey: PIYCZWMJRKZNLW-YYLMEPJHSA-N

SMILES: O[C@H]1[C@@]2([H])[C@](CO[C@@H](C3=CC=CC=C3)O2)([H])O/C([C@@H]1NC(C)=O)=N/O

Biological Activity: 2-Acetamido-4,6-O-benzylidene-2-deoxy-D-gluconohydroximo-1,5-lactone 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-W698874
2-Acetamido-4,6-O-benzylidene-2-deoxy-D-gluconohydroximo-1,5-lactone 2-Acetamido-4,6-O-benzylidene-2-deoxy-D-gluconohydroximo-1,5-lactone 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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