Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
23014
CAS Number:
60117-35-3
N- (5-azido-2-nitrobenzoyloxy)succinimide
Purity:
≥ 99% (RMN)
Synonym(s):
ANB-NOS, Ester N -hydroxysuccinimide de l'acide 5-azido-2-nitrobenzoïque
Documents
$168.35 /100 mg
Taille
Request Bulk Quote
Informations sur le produit

N-(5-Azido-2-nitrobenzoyloxy)succinimide is a versatile compound widely utilized in bioconjugation and chemical biology applications. This compound features an azido group, which is highly reactive and can participate in click chemistry, making it an excellent choice for labeling biomolecules, such as proteins and nucleic acids. Its unique structure allows for selective modifications, enabling researchers to create targeted drug delivery systems and study complex biological interactions. The nitrobenzoyloxy moiety enhances its solubility and stability, further expanding its utility in various experimental setups.

In addition to its applications in research, N-(5-Azido-2-nitrobenzoyloxy)succinimide is also valuable in the development of diagnostic tools and therapeutic agents. Its ability to facilitate the attachment of fluorescent tags or other functional groups allows for enhanced imaging and tracking of biological processes. This compound stands out due to its ease of use and compatibility with a range of substrates, making it a preferred choice for professionals in the fields of medicinal chemistry and molecular biology.

Numéro CAS 
60117-35-3
Formule moléculaire
C11H7N5O6
Poids moléculaire 
305.21
Point de fusion 
129-135 °C
Informations générales
Numéro CAS 
60117-35-3
Formule moléculaire
C11H7N5O6
Poids moléculaire 
305.21
Point de fusion 
129-135 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

N-(5-Azido-2-nitrobenzoyloxy)succinimide is widely utilized in research focused on:

  • Bioconjugation: This compound serves as an effective linker in bioconjugation processes, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing the development of targeted therapies.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for synthesizing novel drug candidates, particularly in creating compounds with improved efficacy and specificity for disease targets.
  • Photochemistry: The azido group enables light-induced reactions, making it valuable in photochemical studies and applications, such as the development of light-activated drug delivery systems.
  • Diagnostics: It is used in the creation of diagnostic tools, including biosensors, where its ability to selectively bind to specific biomolecules can enhance detection methods for various diseases.
  • Polymer Chemistry: This compound is utilized in polymer synthesis, particularly in creating functionalized polymers that can be used in drug delivery systems or as scaffolds in tissue engineering.

Citations