65729-83-1

4-O-Acetyl-2,5-anhydro-1,3-O-isopropylidene-6-trityl-D-glucitol Chemical Structure
65729-83-1

Chemical Structure

4-O-Acetyl-2,5-anhydro-1,3-O-isopropylidene-6-trityl-D-glucitol

  • CAS No.: 65729-83-1
  • Formula:C30H32O6
  • Molecular Weight:488.57

IUPAC Name: (4aS,6R,7R,7aR)-2,2-dimethyl-6-((trityloxy)methyl)tetrahydro-4H-furo[3,2-d][1,3]dioxin-7-yl acetate

InChIKey: SOENFNIYAKGMHW-JUDWXZBOSA-N

SMILES: CC(O[C@@H]([C@@]1([H])[C@@](COC(C)(O1)C)([H])O2)[C@H]2COC(C3=CC=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5)=O

Biological Activity: 4-O-Acetyl-2,5-anhydro-1,3-O-isopropylidene-6-trityl-D-glucitol 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-W698981
4-O-Acetyl-2,5-anhydro-1,3-O-isopropylidene-6-trityl-D-glucitol 4-O-Acetyl-2,5-anhydro-1,3-O-isopropylidene-6-trityl-D-glucitol 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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