14233-48-8
Chemical Structure
2,3,4,6-Tetra-O-benzyl-D-glucitol
- CAS No.: 14233-48-8
- Formula:C34H38O6
- Molecular Weight:542.66
IUPAC Name: (2S,3R,4R,5R)-2,3,4,6-tetrakis(benzyloxy)hexane-1,5-diol
InChIKey: MQOUZFJJURBWAX-KMKAFXEASA-N
SMILES: O[C@H](COCC1=CC=CC=C1)[C@@H](OCC2=CC=CC=C2)[C@H](OCC3=CC=CC=C3)[C@H](CO)OCC4=CC=CC=C4
Biological Activity: 2,3,4,6-Tetra-O-benzyl-D-glucitol 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2,3,4,6-Tetra-O-benzyl-D-glucitol | 2,3,4,6-Tetra-O-benzyl-D-glucitol 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...
/
|
|||||||||||||||||||||||
Keywords