3969-61-7
Chemical Structure
2,3:5,6-Di-O-isopropylidene-D-mannitol
- CAS No.: 3969-61-7
- Formula:C12H22O6
- Molecular Weight:262.30
IUPAC Name: (R)-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)((4S,5R)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol
InChIKey: CKMMCZAVXJINCZ-ZYUZMQFOSA-N
SMILES: O[C@H]([C@@]1([H])COC(C)(O1)C)[C@@]2([H])[C@H](OC(C)(O2)C)CO
Biological Activity: 2,3:5,6-Di-O-isopropylidene-D-mannitol 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2,3:5,6-Di-O-isopropylidene-D-mannitol | 2,3:5,6-Di-O-isopropylidene-D-mannitol 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...
/
|
|||||||||||||||||||||||