855662-12-3
Chemical Structure
Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose
- CAS No.: 855662-12-3
- Formula:C27H23BrO7
- Molecular Weight:539.37
IUPAC Name: (3S,4R,5R,6S)-2-bromo-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate
InChIKey: ZNQXFYBHGDPZCZ-QTDWSHGNSA-N
SMILES: C[C@H]1[C@H]([C@H]([C@@H](C(O1)Br)OC(C2=CC=CC=C2)=O)OC(C3=CC=CC=C3)=O)OC(C4=CC=CC=C4)=O
Biological Activity: Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose | Bromo 2,3,4-Tri-O-benzoyl-L-fucopyranose 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...
/
|
|||||||||||||||||||||||