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Catalog Number:
28218
CAS Number:
6205-69-2
3,4,6-triacétate d'azoture de 2-acétamido-2-désoxy-β-D-glucopyranosyle
Purity:
≥ 99 % (HPLC)
Documents
$106.96 /1G
Taille
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Informations sur le produit

2-Acetamido-2-deoxy-b-D-glucopyranosyl azide 3,4,6-triacetate is a versatile compound with significant applications in the fields of biochemistry and medicinal chemistry. This azide derivative of glucopyranoside is particularly valuable for researchers involved in glycoscience, as it serves as a key intermediate in the synthesis of glycosylated compounds. Its unique structure allows for selective reactions, making it an excellent candidate for click chemistry applications, which are essential in drug development and the creation of complex biomolecules.

Moreover, the compound's triacetate groups enhance its solubility and stability, facilitating its use in various organic synthesis processes. Researchers can leverage its properties to explore new pathways in carbohydrate chemistry, potentially leading to the development of novel therapeutics or diagnostic tools. With its ability to participate in bioorthogonal reactions, this compound opens up exciting possibilities for targeted drug delivery and the study of glycan interactions in biological systems.

Numéro CAS 
6205-69-2
Formule moléculaire
C14H20N4O8
Poids moléculaire 
372.33
Rotation optique 
[a] D 20 = -47 ± 2º (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
6205-69-2
Formule moléculaire
C14H20N4O8
Poids moléculaire 
372.33
Rotation optique 
[a] D 20 = -47 ± 2º (C = 1 dans CHCl 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

2-Acetamido-2-deoxy-b-D-glucopyranosyl azide 3,4,6-triacetate is widely utilized in research focused on:

  • Glycobiology: This compound plays a crucial role in the study of carbohydrate structures and functions, aiding researchers in understanding glycoproteins and their interactions in biological systems.
  • Drug Development: Its azide group allows for click chemistry applications, facilitating the synthesis of new pharmaceutical compounds, which can lead to more effective drugs with fewer side effects.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the development of targeted therapies and diagnostic tools in medicine.
  • Polymer Chemistry: It serves as a building block for creating functionalized polymers, which can be applied in various industries, including biomedical devices and drug delivery systems.
  • Analytical Chemistry: This chemical is useful in the development of assays and detection methods, providing researchers with tools to analyze complex biological samples more effectively.

Citations