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Catalog Number:
05755
CAS Number:
264276-42-8
Fmoc-4-fluoro-DL-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-DL-Phe(4-F)-OH, Fmoc-p - fluoro-DL-Phe-OH, ( Acide RS -Fmoc-2-amino-3-(4-fluorophényl)propionique
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$117.78 /1G
Taille
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Informations sur le produit

Fmoc-4-fluoro-DL-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a fluorine atom on the phenyl ring, enhances its reactivity and stability, making it an attractive choice for researchers in medicinal chemistry and biochemistry.

In practical applications, Fmoc-4-fluoro-DL-phenylalanine is particularly valuable in the synthesis of bioactive peptides, which can be used in therapeutic agents targeting various diseases. Its ability to facilitate the incorporation of fluorinated amino acids into peptides allows for the development of compounds with improved pharmacological properties. This compound is also instrumental in the study of protein interactions and the design of novel biomolecules, providing researchers with a powerful tool for advancing their work in drug discovery and development.

Numéro CAS 
264276-42-8
Formule moléculaire
C 24 H 20 FNO 4
Poids moléculaire 
405.4
Point de fusion 
182-188 °C
Informations générales
Numéro CAS 
264276-42-8
Formule moléculaire
C 24 H 20 FNO 4
Poids moléculaire 
405.4
Point de fusion 
182-188 °C
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

Fmoc-4-fluoro-DL-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the incorporation of fluorinated amino acids that can enhance the stability and bioactivity of the resulting peptides.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing novel drugs, especially those targeting specific biological pathways where fluorine substitution can improve pharmacokinetics.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of peptides to other biomolecules, which is crucial for creating targeted therapies and diagnostic agents.
  • Research in Protein Engineering: Researchers utilize this compound to study protein folding and stability, as the fluorine atom can influence the interactions within protein structures, providing insights into protein behavior.
  • Fluorinated Compound Studies: It serves as a model compound in studies exploring the effects of fluorination on biological activity, helping scientists understand how modifications can lead to improved therapeutic profiles.

Citations