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Catalog Number:
30514
CAS Number:
880637-82-1
Acide Na-Azido-Nb-Fmoc-L-2,3-diaminopropionique
Purity:
≥ 99 % (HPLC)
Synonym(s):
( Acide S -2-azido-3-(Fmoc-amino)propionique, N3-L-Dap(Fmoc)-OH
Documents
$65.40 /100 mg
Taille
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Product Information

Dérivé d'acide 2,3-diaminopropanoïque protégé orthogonalement utile ; voir Virta et al., J.Org.Chem., 2006, 71(5), 1989-1999. Attention à la procédure de couplage à faible racémisation modifiée.

Synonyms
( Acide S -2-azido-3-(Fmoc-amino)propionique, N3-L-Dap(Fmoc)-OH
CAS Number
880637-82-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C18H16N4O4
Molecular Weight
352.3
MDL Number
MFCD22989449
PubChem ID
72988743
Appearance
Poudre cristalline blanche
Optical Rotation
C18H16N4O4
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( Acide S -2-azido-3-(Fmoc-amino)propionique, N3-L-Dap(Fmoc)-OH
CAS Number
880637-82-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C18H16N4O4
Molecular Weight
352.3
MDL Number
MFCD22989449
PubChem ID
72988743
Appearance
Poudre cristalline blanche
Optical Rotation
C18H16N4O4
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na-Azido-Nb-Fmoc-L-2,3-diaminopropionic 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 the development of novel therapeutic agents.
  • Drug Development: Its unique azido group allows for click chemistry applications, facilitating the creation of complex drug molecules with improved efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and targeted therapies.
  • Research in Neuroscience: It is employed in studies involving neuropeptides, aiding in the understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Material Science: The azido functionality allows for the modification of polymers, enhancing their properties for applications in coatings and drug delivery systems.

Citations