20689-02-5
Chemical Structure
Phenylmethyl 2,3:5,6-bis-O-(1-methylethylidene)-α-D-mannofuranoside
- CAS No.: 20689-02-5
- Formula:C19H26O6
- Molecular Weight:350.41
IUPAC Name: (3aS,4S,6R,6aS)-4-(benzyloxy)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole
InChIKey: FDOXFJBHCHWEOL-NRKLIOEPSA-N
SMILES: CC(C)(O1)O[C@@]2([H])[C@]1([H])[C@]([C@]3([H])OC(C)(OC3)C)([H])O[C@@H]2OCC4=CC=CC=C4
Biological Activity: Phenylmethyl 2,3:5,6-bis-O-(1-methylethylidene)-α-D-mannofuranoside 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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Phenylmethyl 2,3:5,6-bis-O-(1-methylethylidene)-α-D-mannofuranoside | Phenylmethyl 2,3:5,6-bis-O-(1-methylethylidene)-α-D-mannofuranoside 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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