65729-88-6
Chemical Structure
D-Mannitol,2,5-anhydro,1,3,4,6-tetraacetate
- CAS No.: 65729-88-6
- Formula:C14H20O9
- Molecular Weight:332.30
IUPAC Name: (2R,3R,4R,5R)-2,5-bis(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
InChIKey: LRVQZSOYVOEEPQ-AAVRWANBSA-N
SMILES: CC(O[C@H]1[C@@H]([C@H](O[C@@H]1COC(C)=O)COC(C)=O)OC(C)=O)=O
Biological Activity: D-Mannitol,2,5-anhydro,1,3,4,6-tetraacetate 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
D-Mannitol,2,5-anhydro,1,3,4,6-tetraacetate | D-Mannitol,2,5-anhydro,1,3,4,6-tetraacetate 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...
/
|
|||||||||||||||||||||||
