Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
21406
CAS Number:
28541-84-6
6-Bromo-2-naphthyl-a-D-mannopyranoside
Synonym(s):
2-(6-Bromonaphthyl)-a-D-mannopyranoside
Documents
Available - Request Bulk Quote
Pack Size Availability Price
Request Bulk Quote
Product Information

6-Bromo-2-naphthyl-α-D-mannopyranoside is a specialized glycoside that has garnered attention in various fields of research and industry due to its unique structural properties and functional versatility. This compound features a brominated naphthalene moiety, which enhances its reactivity and potential applications in synthetic organic chemistry. Its ability to act as a glycosyl donor makes it particularly valuable in the synthesis of complex carbohydrates and glycoproteins, which are crucial in biochemistry and pharmaceutical research. Researchers have utilized this compound in the development of targeted drug delivery systems and in the study of carbohydrate-protein interactions, showcasing its relevance in the advancement of therapeutic strategies.

In addition to its applications in organic synthesis, 6-Bromo-2-naphthyl-α-D-mannopyranoside serves as a useful tool in the exploration of enzyme mechanisms and the design of carbohydrate-based materials. Its unique properties allow for the modification of biological pathways, making it an essential compound for those engaged in glycoscience and related fields. The compound's stability and reactivity profile provide a significant advantage over similar glycosides, making it a preferred choice for researchers looking to innovate in carbohydrate chemistry.

Synonyms
2-(6-Bromonaphthyl)-a-D-mannopyranoside
CAS Number
28541-84-6
Molecular Formula
C16H17BrO6
Molecular Weight
385.21
MDL Number
MFCD00067621
PubChem ID
119836
Conditions
Store at 0-8°C
General Information
Synonyms
2-(6-Bromonaphthyl)-a-D-mannopyranoside
CAS Number
28541-84-6
Molecular Formula
C16H17BrO6
Molecular Weight
385.21
MDL Number
MFCD00067621
PubChem ID
119836
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Bromo-2-naphthyl-a-D-mannopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic organic chemistry, facilitating the formation of glycosidic bonds, which are essential in creating complex carbohydrates.
  • Biochemical Research: It is used in studies involving carbohydrate-binding proteins, helping researchers understand interactions between sugars and proteins, which is crucial in fields like enzymology and drug design.
  • Drug Development: The compound's unique structure allows it to be explored as a potential lead compound in developing new therapeutics targeting glycan-related diseases, such as certain cancers and infections.
  • Fluorescent Probes: Due to its naphthalene moiety, it can be utilized in creating fluorescent probes for monitoring biological processes, enhancing imaging techniques in cellular biology.
  • Material Science: It can be incorporated into polymer matrices to improve the properties of materials, such as enhancing biocompatibility for biomedical applications.

Citations