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Catalog Number:
30472
CAS Number:
763139-35-1
Sel de cyclohexylammonium de N α -Boc-N δ -Azido-L-Ornithine
Purity:
>98%
Synonym(s):
( S -Boc-2-amino-5-azido-pentanoïque acide cyclohexylaminesel, Boc-Orn(N3)-OH·CHA
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$58.39 /100 mg
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Informations sur le produit

Na-Boc-Nd-Azido-L-Ornithine cyclohexylammonium salt is a versatile compound widely utilized in the fields of biochemistry and medicinal chemistry. This compound features a unique azido group, which enhances its reactivity and makes it an excellent candidate for click chemistry applications. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex molecules. Researchers often leverage this compound in the development of peptide-based therapeutics and in the study of protein interactions, where its azido functionality can be employed for labeling and tracking biomolecules.

In addition to its applications in drug discovery, Na-Boc-Nd-Azido-L-Ornithine cyclohexylammonium salt is also valuable in the synthesis of novel materials and in the exploration of new chemical pathways. Its stability and ease of handling make it a preferred choice for laboratories focused on innovative research. By incorporating this compound into your projects, you can enhance your research capabilities and drive forward your scientific endeavors.

Numéro CAS 
763139-35-1
Formule moléculaire
C16H31N5O4
Poids moléculaire 
357.4
Informations générales
Numéro CAS 
763139-35-1
Formule moléculaire
C16H31N5O4
Poids moléculaire 
357.4
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

Na-Boc-Nd-Azido-L-Ornithine cyclohexylammonium salt is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those with azide functionalities, enabling researchers to create complex structures for drug development.
  • Click Chemistry: Its azido group allows for efficient click chemistry reactions, facilitating the conjugation of biomolecules, which is essential in creating targeted therapies and diagnostics.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs or imaging agents to proteins, enhancing their efficacy and specificity in therapeutic applications.
  • Research in Drug Delivery: It plays a role in developing novel drug delivery systems, where its unique properties can improve the stability and release profiles of therapeutic agents.
  • Biomedical Research: The compound is valuable in biomedical research for studying cellular processes and interactions, providing insights that can lead to advancements in disease treatment.

Citations