19131-06-7

1,2:5,6-Di-O-isopropylidene-3-O-tosyl-α-D-gulofuranose Chemical Structure
19131-06-7

Chemical Structure

1,2:5,6-Di-O-isopropylidene-3-O-tosyl-α-D-gulofuranose

  • CAS No.: 19131-06-7
  • Formula:C19H26O8S
  • Molecular Weight:414.47

IUPAC Name: (3aR,5S,6R,6aR)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate

InChIKey: FOVFLADZRUACHW-ZHCJQAHYSA-N

SMILES: O=S(O[C@@H]1[C@@]([C@@]2([H])COC(C)(O2)C)([H])O[C@@]3([H])[C@]1([H])OC(C)(O3)C)(C4=CC=C(C=C4)C)=O

Biological Activity: 1,2:5,6-Di-O-isopropylidene-3-O-tosyl-α-D-gulofuranose 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-W416007
1,2:5,6-Di-O-isopropylidene-3-O-tosyl-α-D-gulofuranose 1,2:5,6-Di-O-isopropylidene-3-O-tosyl-α-D-gulofuranose 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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