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Catalog Number:
21475
CAS Number:
69594-75-8
6-Bromo-2-naphtyl-β-D-xylopyranoside
Synonym(s):
2-(6-bromonaphtyl)-β-D-xylopyranoside
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Product Information

6-Bromo-2-naphthyl-β-D-xylopyranoside is a specialized glycoside that has garnered attention in various fields of research and industry due to its unique structural properties and biological activity. This compound is particularly notable for its potential applications in the study of enzyme interactions and carbohydrate recognition processes. Researchers have utilized 6-Bromo-2-naphthyl-β-D-xylopyranoside as a substrate in glycosidase assays, enabling the exploration of enzyme kinetics and mechanisms. Its bromonaphthyl group enhances fluorescence, making it an excellent candidate for use in biochemical assays and imaging studies.

In addition to its utility in enzymatic studies, this compound can serve as a valuable tool in the development of glycosylation reactions, which are crucial in the synthesis of complex carbohydrates and glycoproteins. The unique properties of 6-Bromo-2-naphthyl-β-D-xylopyranoside provide researchers with a versatile compound that can facilitate advancements in glycoscience, drug development, and biochemistry. Its ability to act as a fluorescent probe further enhances its appeal for applications in molecular biology and analytical chemistry.

Synonyms
2-(6-bromonaphtyl)-β-D-xylopyranoside
CAS Number
69594-75-8
Molecular Formula
C 15 H 15 BrO 5
Molecular Weight
355.18
MDL Number
MFCD00076065
PubChem ID
53398696
Conditions
Conserver à 0-8°C
General Information
Synonyms
2-(6-bromonaphtyl)-β-D-xylopyranoside
CAS Number
69594-75-8
Molecular Formula
C 15 H 15 BrO 5
Molecular Weight
355.18
MDL Number
MFCD00076065
PubChem ID
53398696
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Bromo-2-naphthyl-b-D-xylopyranoside is widely utilized in research focused on:

  • Glycosylation Studies: This compound serves as a valuable substrate in glycosylation reactions, helping researchers understand carbohydrate chemistry and enzyme interactions.
  • Drug Development: Its unique structure makes it a candidate for designing new pharmaceuticals, particularly in targeting specific biological pathways in diseases.
  • Biochemical Assays: It is used in various assays to evaluate enzyme activity, providing insights into metabolic processes and potential therapeutic targets.
  • Fluorescent Probes: The compound can be modified to create fluorescent labels for tracking biological molecules, enhancing imaging techniques in cellular biology.
  • Material Science: It finds applications in developing novel materials, particularly in creating functionalized polymers that have specific chemical properties.

Citations