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Catalog Number:
16738
CAS Number:
1217777-84-8
Fmoc-α-méthyl-D-4-fluorophénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-α-Me-D-Phe(4-F)-OH, Acide Fmoc-( R )-2-amino-2-méthyl-3-(4-fluorophényl)propanoïque
Documents
$70.00 /100 mg
Taille
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Informations sur le produit

Fmoc-a-methyl-D-4-fluorophenylalanine is a valuable 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 4-fluorophenyl group, enhances its utility in the development of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to improve the stability and solubility of peptides, making it an ideal choice for applications in medicinal chemistry and biochemistry.

In addition to its role in peptide synthesis, Fmoc-a-methyl-D-4-fluorophenylalanine is also employed in the study of protein interactions and enzyme activity due to its fluorinated aromatic side chain, which can influence binding properties. Its versatility and effectiveness in various applications make it a preferred choice for professionals in the pharmaceutical and biotechnology industries, particularly those focused on developing novel therapeutics and conducting advanced research.

Numéro CAS 
1217777-84-8
Formule moléculaire
C 25 H 22 FNO 4
Poids moléculaire 
419.44
Point de fusion 
66 - 72 °C
Rotation optique 
[a] D 25 = 23 ± 1 º (C = 1 dans DMF) D 25 = -6 ± 1 º (C = 1 dans EtOH)
Informations générales
Numéro CAS 
1217777-84-8
Formule moléculaire
C 25 H 22 FNO 4
Poids moléculaire 
419.44
Point de fusion 
66 - 72 °C
Rotation optique 
[a] D 25 = 23 ± 1 º (C = 1 dans DMF) D 25 = -6 ± 1 º (C = 1 dans EtOH)
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-a-methyl-D-4-fluorophenylalanine 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, enhancing the efficiency and yield of the process.
  • Drug Development: Its unique structural properties make it valuable in the design of novel pharmaceuticals, especially in targeting specific biological pathways, which can lead to more effective treatments.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing biosensors and targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter systems, helping researchers understand the role of specific amino acids in brain function and potential therapeutic targets for neurological disorders.
  • Fluorescent Labeling: The fluorine atom in its structure allows for fluorescent labeling, enabling visualization in various biological assays, which aids in tracking molecular interactions in real-time.

Citations