383173-65-7

Benzyl 2,3,4-Tri-O-acetyl-4-nitromethyl-β-D-arabinopyranoside Chemical Structure
383173-65-7

Chemical Structure

Benzyl 2,3,4-Tri-O-acetyl-4-nitromethyl-β-D-arabinopyranoside

  • CAS No.: 383173-65-7
  • Formula:C19H23NO10
  • Molecular Weight:425.39

IUPAC Name: (2R,3S,4S,5R)-2-(benzyloxy)-5-(nitromethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

InChIKey: ADINWQVDJMMULQ-INDMIFKZSA-N

SMILES: O=[N+]([O-])C[C@@]1([C@H]([C@@H]([C@@H](OC1)OCC2=CC=CC=C2)OC(C)=O)OC(C)=O)OC(C)=O

Biological Activity: Benzyl 2,3,4-Tri-O-acetyl-4-nitromethyl-β-D-arabinopyranoside 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-W699199
Benzyl 2,3,4-Tri-O-acetyl-4-nitromethyl-β-D-arabinopyranoside Benzyl 2,3,4-Tri-O-acetyl-4-nitromethyl-β-D-arabinopyranoside 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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