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Catalog Number:
28908
CAS Number:
19285-38-2
β-D-Galactopyranosyl bromide,2,3,4,6-tetraacetate
Synonym(s):
1-Bromo-2,3,4,6-tetra-acetyl-β-D-galactoside
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Product Information

b-D-Galactopyranosyl bromide, 2,3,4,6-tetraacetate is a versatile glycosyl donor that plays a crucial role in carbohydrate chemistry and biochemistry. This compound is particularly valued for its ability to facilitate the synthesis of complex oligosaccharides and glycoconjugates, making it an essential tool for researchers in the fields of glycoscience and medicinal chemistry. Its unique structure, featuring multiple acetyl groups, enhances its stability and reactivity, allowing for efficient glycosylation reactions.

In practical applications, b-D-Galactopyranosyl bromide, 2,3,4,6-tetraacetate is utilized in the development of glycosylated drugs and vaccines, where precise carbohydrate structures are critical for biological activity and efficacy. Additionally, it serves as a valuable intermediate in the synthesis of glycoproteins and glycolipids, which are vital for cell signaling and recognition processes. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and achieve higher yields in their carbohydrate-based projects.

Synonyms
1-Bromo-2,3,4,6-tetra-acetyl-β-D-galactoside
CAS Number
19285-38-2
Molecular Formula
C14H19BrO9
Molecular Weight
411.2
MDL Number
MFCD05864887
PubChem ID
102932
Conditions
Store at 0-8°C
General Information
Synonyms
1-Bromo-2,3,4,6-tetra-acetyl-β-D-galactoside
CAS Number
19285-38-2
Molecular Formula
C14H19BrO9
Molecular Weight
411.2
MDL Number
MFCD05864887
PubChem ID
102932
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

b-D-Galactopyranosyl bromide, 2,3,4,6-tetraacetate is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in organic synthesis, enabling the formation of glycosidic bonds. It is particularly valuable in the synthesis of complex carbohydrates and glycoproteins, which are essential in biochemistry and pharmaceuticals.
  • Bioconjugation: It is used in bioconjugation techniques to attach carbohydrates to proteins or other biomolecules. This application is crucial in developing targeted drug delivery systems and enhancing the efficacy of therapeutic agents.
  • Research in Cell Biology: The compound aids in studying cell signaling and recognition processes by mimicking natural glycan structures. This is important for understanding cellular interactions and developing new therapeutic strategies.
  • Vaccine Development: Its role in synthesizing glyco-conjugate vaccines highlights its significance in immunology. By linking sugars to proteins, it helps create vaccines that can elicit stronger immune responses.
  • Diagnostic Applications: The compound can be utilized in developing diagnostic tools that rely on glycan recognition, enhancing the specificity and sensitivity of tests for various diseases.

Citations