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Catalog Number:
29622
CAS Number:
1485528-98-0
Sel de dicyclohexylammonium de l'acide S -Boc-2-amino-5-azido-pentanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-Orn(N3)-OH·DCHA
Documents
$79.22 /25 mg
Taille
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Informations sur le produit

(S)-Boc-2-amino-5-azido-pentanoic acid dicyclohexylammonium salt is a versatile compound that serves as a valuable building block in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is crucial for the selective protection of amines during chemical reactions. Its azido group allows for further functionalization through click chemistry, making it an excellent candidate for applications in bioconjugation and drug development. Researchers can leverage its unique properties to create novel peptides and explore potential therapeutic agents, particularly in the fields of oncology and infectious diseases.

The dicyclohexylammonium salt form enhances solubility and stability, facilitating easier handling and incorporation into various formulations. This compound is particularly relevant for professionals engaged in synthetic organic chemistry, as it streamlines the synthesis of complex molecules. Its ability to undergo diverse chemical transformations positions it as a key player in the development of innovative therapeutic strategies, offering significant advantages over similar compounds by providing enhanced reactivity and functionalization options.

Numéro CAS 
1485528-98-0
Formule moléculaire
C10H18N4O4 · C12H23N
Poids moléculaire 
439.6
Rotation optique 
[α] D 20 = +14 ± 2º (C=1, en MeOH)
Informations générales
Numéro CAS 
1485528-98-0
Formule moléculaire
C10H18N4O4 · C12H23N
Poids moléculaire 
439.6
Rotation optique 
[α] D 20 = +14 ± 2º (C=1, en MeOH)
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

(S)-Boc-2-amino-5-azido-pentanoic acid dicyclohexylammonium salt is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of modified peptides that can enhance biological activity or stability.
  • Drug Development: It plays a significant role in pharmaceutical research, especially in the design of new drugs that target specific biological pathways, thanks to its unique functional groups.
  • Bioconjugation: The azido group allows for click chemistry applications, facilitating the attachment of various biomolecules, which is crucial in creating targeted therapies and diagnostics.
  • Research in Neuroscience: Its derivatives are being explored for potential applications in neurobiology, particularly in studying neurotransmitter interactions and signaling pathways.
  • Material Science: This compound can be used in the development of novel materials with specific properties, such as hydrogels or polymers that respond to environmental stimuli.

Citations