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Catalog Number:
32327
CAS Number:
68733-20-0
1,3,4,6-Tétra- O -acétyl-2-azido-2-désoxy-α-D-mannopyranose
Purity:
≥ 95 % (HPLC)
Documents
$175.00 /100 mg
Taille
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Informations sur le produit

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a versatile compound widely utilized in carbohydrate chemistry and bioconjugation applications. This azido sugar derivative is particularly valuable for researchers focused on glycoscience, as it serves as a key intermediate in the synthesis of glycosylated compounds. Its unique azido functional group allows for efficient click chemistry reactions, enabling the formation of stable linkages with various biomolecules, which is essential in the development of targeted drug delivery systems and diagnostic tools.

Moreover, the acetyl protecting groups enhance the compound's stability and solubility, making it easier to handle in laboratory settings. This compound is also instrumental in the synthesis of glycoproteins and glycolipids, which play critical roles in cell signaling and recognition processes. With its broad applicability in synthetic organic chemistry and potential in biomedical research, 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose stands out as a crucial tool for advancing research in glycosylation and related fields.

Numéro CAS 
68733-20-0
Formule moléculaire
C14H19N3O9
Poids moléculaire 
373.32
Rotation optique 
[a] D 20 3 )
Informations générales
Numéro CAS 
68733-20-0
Formule moléculaire
C14H19N3O9
Poids moléculaire 
373.32
Rotation optique 
[a] D 20 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-a-D-mannopyranose is widely utilized in research focused on:

  • Carbohydrate Chemistry: This compound serves as a key intermediate in synthesizing various glycosylated compounds, aiding researchers in exploring carbohydrate structures and functions.
  • Drug Development: Its azido group allows for click chemistry applications, facilitating the development of novel pharmaceuticals through efficient conjugation methods.
  • Bioconjugation: The compound is employed in bioconjugation processes to attach biomolecules, enhancing the targeting and efficacy of drug delivery systems.
  • Diagnostics: It can be used in the creation of diagnostic agents, particularly in imaging techniques that require specific carbohydrate recognition.
  • Material Science: The compound's unique properties make it suitable for developing functionalized materials, such as hydrogels, which can be tailored for biomedical applications.

Citations