91364-12-4
Chemical Structure
Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose
- CAS No.: 91364-12-4
- Formula:C35H34O6
- Molecular Weight:550.64
IUPAC Name: 1-((3aR,4S,6S,6aS)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-2-(trityloxy)ethan-1-one
InChIKey: SFFSXRAQVHMPKF-GJBCSVNNSA-N
SMILES: O=C([C@@H]1[C@@]2([H])[C@@](OC(C)(O2)C)([H])[C@H](O1)OCC3=CC=CC=C3)COC(C4=CC=CC=C4)(C5=CC=CC=C5)C6=CC=CC=C6
Biological Activity: Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose 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].
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Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose | Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose 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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