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Catalog Number:
30535
CAS Number:
1229394-75-5
2 R ,3 R -(Fmoc-amino)-3-acide azidobutyrique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Abu(3 R -N3)-OH
Antibiotic
Documents
$93.14 /100 mg
Taille
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Informations sur le produit

Dérivé protégé pour la synthèse de peptides contenant de l'acide 2,3-diaminobutanoïque et également pour les réactions de clic.

Numéro CAS 
1229394-75-5
Formule moléculaire
C19H18N4O4
Poids moléculaire 
366.4
Point de fusion 
147-154 °C
Rotation optique 
[a] D 20 = -13 ± 2º (C=1 dans MeOH)
Informations générales
Numéro CAS 
1229394-75-5
Formule moléculaire
C19H18N4O4
Poids moléculaire 
366.4
Point de fusion 
147-154 °C
Rotation optique 
[a] D 20 = -13 ± 2º (C=1 dans 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

(2R,3R)-(Fmoc-amino)-3-azidobutyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the incorporation of azido groups that can facilitate further modifications.
  • Bioconjugation: Its azido group enables click chemistry applications, making it ideal for bioconjugation processes in drug development and diagnostics, enhancing the specificity and efficacy of therapeutic agents.
  • Drug Development: Researchers leverage this compound in the design of novel drug candidates, particularly in the development of targeted therapies that require precise molecular interactions.
  • Material Science: The compound can be used to create functionalized polymers and materials, which are valuable in creating smart materials with specific properties for various applications, including sensors and drug delivery systems.
  • Biological Research: It is instrumental in studying protein interactions and cellular processes, providing insights that can lead to advancements in understanding diseases and developing new treatment strategies.

Citations