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Catalog Number:
30532
CAS Number:
131669-42-6
Acide (2 S ,3 S )-(Fmoc-amino)-3-azidobutyrique
Purity:
≥ 99 % (HPLC, CCM)
Synonym(s):
Fmoc-L-Abu( 3S -N3)-OH
Antibiotic
Documents
$98.10 /100 mg
Taille
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Product Information

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

Synonyms
Fmoc-L-Abu( 3S -N3)-OH
CAS Number
131669-42-6
Purity
≥ 99 % (HPLC, CCM)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363164
PubChem ID
14683492
Melting Point
151 - 152 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = 13 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Abu( 3S -N3)-OH
CAS Number
131669-42-6
Purity
≥ 99 % (HPLC, CCM)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363164
PubChem ID
14683492
Melting Point
151 - 152 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = 13 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Oui
DEA-regulated
Non
Warnings
-
Applications

(2S,3S)-(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 the development of novel therapeutic agents. Its unique azido group allows for further modifications, enhancing the versatility of peptide design.
  • Click Chemistry: The azido functional group enables applications in click chemistry, facilitating the efficient and selective coupling of biomolecules. This is particularly useful in drug discovery and bioconjugation processes.
  • Biotechnology: In the field of biotechnology, it is used to create modified proteins and enzymes, improving their stability and activity. This can lead to more effective biocatalysts for industrial processes.
  • Drug Development: Researchers leverage this compound in the development of new drugs, particularly in targeting specific diseases. Its ability to incorporate into larger molecular frameworks makes it valuable in medicinal chemistry.
  • Diagnostic Applications: The compound can be utilized in the development of diagnostic tools, such as imaging agents or biosensors, due to its reactive azido group that can be linked to various detection systems.

Citations