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Catalog Number:
15120
CAS Number:
220497-48-3
Fmoc-3-bromo-L-phénylalanine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-L-Phe(3-Br)-OH, Fmoc-3-bromo-L-Phe-OH, ( Acide S -2-Fmoc-2-amino-3-(3-bromophényl)propionique
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$86.23 /1G
Taille
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Informations sur le produit

Fmoc-3-bromo-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which enhances its stability and solubility, making it an excellent choice for solid-phase peptide synthesis. Its bromine substitution at the phenyl group allows for further functionalization, enabling researchers to explore a variety of chemical modifications that can lead to novel therapeutic agents.

In the pharmaceutical industry, Fmoc-3-bromo-L-phenylalanine is particularly valuable for the synthesis of bioactive peptides, which are crucial in developing new drugs for various diseases. Its ability to facilitate the introduction of specific functionalities into peptide chains opens up possibilities for creating targeted therapies and improving drug efficacy. Researchers appreciate its ease of use and the efficiency it brings to peptide synthesis, making it a preferred choice for both academic and industrial applications.

Numéro CAS 
220497-48-3
Formule moléculaire
C24H20BrNO4
Poids moléculaire 
466.3
Informations générales
Numéro CAS 
220497-48-3
Formule moléculaire
C24H20BrNO4
Poids moléculaire 
466.3
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-3-bromo-L-phenylalanine 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 (SPPS), allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in medicinal chemistry, where its unique bromine substituent can enhance the biological activity of peptide-based drugs, making it valuable in the pharmaceutical industry.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it can be attached to biomolecules, facilitating the development of targeted drug delivery systems or diagnostic agents.
  • Research in Protein Engineering: It is employed in studies aimed at modifying protein structures, helping scientists understand protein function and stability, which is crucial in biotechnology and enzyme engineering.
  • Fluorescent Labeling: Fmoc-3-bromo-L-phenylalanine can be used in fluorescent labeling applications, aiding in the visualization of peptides in biological assays, which is essential for various research applications.

Citations