5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE
5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE Basic information
- Product Name:
- 5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE
- Synonyms:
-
- 5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE
- Magenta-alpha-glucoside
- Magenta-α-D-Glc
- (2R,3R,4S,5S,6R)-2-((5-bromo-6-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- CAS:
- 878495-64-8
- MF:
- C14H15BrClNO6
- MW:
- 408.63
- Product Categories:
-
- substrate
- Mol File:
- Mol File
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5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE Chemical Properties
- form
- powder
- color
- White
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Safety Information
- Hazard Codes
- Xi
- HS Code
- 2940000080
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5-BROMO-6-CHLORO-3-INDOLYL ALPHA-D-GLUCOPYRANOSIDE Usage And Synthesis
Uses
5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside 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].
References
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922
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