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Catalog Number:
32257
CAS Number:
140428-81-5
2-Azidoéthyl 2,3,4,6-tétra -O -acétyl-β-D-glucopyranoside
Purity:
Point unique (TLC)
Documents
$100.05 /100 mg
Taille
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Informations sur le produit

2-Azidoethyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is a versatile compound widely utilized in the fields of organic synthesis and bioconjugation. This azido sugar derivative is particularly valuable for researchers focusing on glycoscience, as it serves as a key building block for the synthesis of glycoproteins and glycolipids. Its unique azide functional group allows for efficient click chemistry reactions, enabling the formation of stable linkages with various biomolecules, which is essential for developing targeted drug delivery systems and diagnostic tools.

The compound's acetyl groups enhance its solubility and stability, making it suitable for a range of applications in medicinal chemistry and biochemistry. Researchers can leverage its properties to create novel glycosylated compounds, facilitating studies in cell signaling and molecular recognition. With its ability to participate in bioorthogonal reactions, 2-Azidoethyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside stands out as a crucial reagent for advancing research in carbohydrate chemistry and related fields.

Numéro CAS 
140428-81-5
Formule moléculaire
C16H23N3O10
Poids moléculaire 
417.37
Point de fusion 
114 - 115 °C
Rotation optique 
[a] 20 D = -33 à -40 ° (C=1,5 dans CHCl 3 )
Informations générales
Numéro CAS 
140428-81-5
Formule moléculaire
C16H23N3O10
Poids moléculaire 
417.37
Point de fusion 
114 - 115 °C
Rotation optique 
[a] 20 D = -33 à -40 ° (C=1,5 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-Azidoethyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is widely utilized in research focused on:

  • Glycobiology: This compound serves as a versatile building block for synthesizing glycoproteins and glycolipids, essential for studying cell-cell interactions and signaling pathways.
  • Drug Development: It is used in the design of carbohydrate-based drugs, enhancing the efficacy and targeting of therapeutic agents in treating diseases such as cancer.
  • Bioconjugation: The azido group allows for click chemistry applications, facilitating the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted drug delivery systems.
  • Diagnostics: This chemical can be employed in the development of diagnostic tools, such as biosensors, that utilize carbohydrate recognition elements for detecting specific biomolecules.
  • Material Science: It finds applications in creating functionalized polymers and materials, which can be tailored for specific properties in biomedical engineering and nanotechnology.

Citations