35023-71-3

β-D-Glucopyranoside,2-chloro-4-nitrophenyl,2,3,4,6-tetraacetate Chemical Structure
35023-71-3

Chemical Structure

β-D-Glucopyranoside,2-chloro-4-nitrophenyl,2,3,4,6-tetraacetate

  • CAS No.: 35023-71-3
  • Formula:C20H22ClNO12
  • Molecular Weight:503.84

IUPAC Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(2-chloro-4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate

InChIKey: QRNIUQCWYQOPLO-OUUBHVDSSA-N

SMILES: CC(O[C@@H]1[C@H]([C@@H](O[C@@H]([C@H]1OC(C)=O)COC(C)=O)OC2=C(C=C(C=C2)[N+]([O-])=O)Cl)OC(C)=O)=O

Biological Activity: β-D-Glucopyranoside,2-chloro-4-nitrophenyl,2,3,4,6-tetraacetate 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-W416311
β-D-Glucopyranoside,2-chloro-4-nitrophenyl,2,3,4,6-tetraacetate β-D-Glucopyranoside,2-chloro-4-nitrophenyl,2,3,4,6-tetraacetate 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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