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Catalog Number:
33460
CAS Number:
1931895-14-5
N 3 -1,4- trans -CHC-OH
Purity:
≥ 99 % (dosage par titration, HPLC)
Synonym(s):
acide trans -4-azidocyclohexanecarboxylique
Antibiotic
Documents
$68.90 /100 mg
Taille
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Informations sur le produit

N3-1,4-trans-CHC-OH, also known as 4-azidocyclohexane-1-carboxylic acid, is a versatile compound with significant potential in various fields, particularly in organic synthesis and medicinal chemistry. This compound features a unique azido group, which makes it an excellent candidate for click chemistry applications, allowing for the efficient formation of diverse chemical structures. Researchers can leverage its properties for the development of novel pharmaceuticals, as the azido functionality can facilitate the introduction of bioactive moieties into drug candidates.

In addition to its applications in drug development, N3-1,4-trans-CHC-OH can also be utilized in materials science for the synthesis of functionalized polymers and nanomaterials. Its ability to undergo selective reactions opens up possibilities for creating advanced materials with tailored properties. The compound's stability and reactivity make it a valuable tool for chemists looking to innovate in both academic and industrial settings, providing a pathway to explore new chemical entities and enhance existing formulations.

Numéro CAS 
1931895-14-5
Formule moléculaire
C7H11N3O2
Poids moléculaire 
169.2
Point de fusion 
70 - 72 °C
Informations générales
Numéro CAS 
1931895-14-5
Formule moléculaire
C7H11N3O2
Poids moléculaire 
169.2
Point de fusion 
70 - 72 °C
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

N3-1,4-trans-CHC-OH is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceutical agents, particularly in developing novel antibiotics and antiviral medications.
  • Bioconjugation: Its azide functional group allows for click chemistry applications, facilitating the attachment of biomolecules for targeted drug delivery systems.
  • Material Science: Used in creating advanced materials, it contributes to the development of polymers with enhanced properties, such as increased strength and thermal stability.
  • Diagnostics: The compound plays a role in the production of diagnostic agents, improving the specificity and sensitivity of imaging techniques in medical applications.
  • Research in Organic Chemistry: It is a valuable reagent for studying reaction mechanisms and developing new synthetic pathways, aiding chemists in exploring innovative chemical transformations.

Citations