22529-61-9
Chemical Structure
3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranose
- CAS No.: 22529-61-9
- Formula:C16H22O6
- Molecular Weight:310.34
IUPAC Name: (R)-1-((3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol
InChIKey: CIFFIYJOTIJKSX-UXXRCYHCSA-N
SMILES: OC[C@@H](O)[C@@]1([H])O[C@@](OC(C)(O2)C)([H])[C@@]2([H])[C@H]1OCC3=CC=CC=C3
Biological Activity: 3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranose 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranose | 3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranose 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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||