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Catalog Number:
42329
2-acétamido-3- O -allyl-4,6- O -benzylidène-2-désoxy-β-D-glucopyranosyl azoture
Purity:
≥ 98 % (HPLC)
Documents
$377.97 /1G
Taille
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Informations sur le produit

2-Acetamido-3-O-allyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is a specialized compound with significant potential in the fields of biochemistry and medicinal chemistry. This compound, characterized by its unique azide functional group, serves as a versatile building block for the synthesis of glycosylated compounds, which are crucial in the development of glycoproteins and other biomolecules. Its structural features allow for selective reactions, making it an ideal candidate for click chemistry applications, particularly in the creation of complex carbohydrate structures that can be used in drug development and targeted therapies.

The compound's ability to participate in bioorthogonal reactions enhances its utility in labeling and tracking biomolecules in live cells, providing researchers with powerful tools for studying cellular processes. Additionally, its stability and reactivity make it suitable for various applications, including the synthesis of glycosylated drugs and the development of diagnostic agents. With its unique properties, 2-Acetamido-3-O-allyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide stands out as a valuable resource for researchers looking to innovate in the fields of glycoscience and pharmaceutical development.

Formule moléculaire
C18H22N4O5
Poids moléculaire 
374.4
Rotation optique 
a 20 D = -78 à -74 ° (C=0,5 dans la pyridine)
Informations générales
Formule moléculaire
C18H22N4O5
Poids moléculaire 
374.4
Rotation optique 
a 20 D = -78 à -74 ° (C=0,5 dans la pyridine)
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-3-O-allyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is widely utilized in research focused on:

  • Glycobiology: This compound serves as a valuable tool for studying carbohydrate-protein interactions, aiding researchers in understanding biological processes like cell signaling and immune responses.
  • Drug Development: Its unique structure allows for the synthesis of glycosylated compounds, which can enhance the efficacy and specificity of therapeutic agents, particularly in targeting cancer cells.
  • Bioconjugation: The azide functional group enables click chemistry applications, facilitating the attachment of biomolecules for creating targeted drug delivery systems or imaging agents.
  • Material Science: It can be incorporated into polymer matrices to develop smart materials with specific properties, such as responsiveness to environmental stimuli, which are useful in various industrial applications.
  • Diagnostics: The compound can be used in the development of diagnostic assays, particularly in detecting specific biomolecules, thus enhancing the accuracy of medical testing.

Citations