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Catalog Number:
07396
CAS Number:
205445-54-1
Boc-3,4,5-trifluoro-L-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Phe(3,4,5-trifluoro)-OH
Documents
$110.57 /250 mg
Taille
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Informations sur le produit

Boc-3,4,5-trifluoro-L-phenylalanine is a specialized amino acid derivative that offers unique properties for various applications in the pharmaceutical and biochemical industries. This compound is particularly valuable for researchers focused on peptide synthesis and drug development, as its trifluoromethyl group enhances lipophilicity and metabolic stability. The Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for complex peptide synthesis.

In addition to its utility in peptide chemistry, Boc-3,4,5-trifluoro-L-phenylalanine can be employed in the design of novel therapeutics, particularly in the development of inhibitors targeting specific enzymes or receptors. Its unique fluorinated structure can lead to compounds with improved pharmacokinetic properties, making it a promising candidate for further research and development. This compound not only facilitates the creation of more effective drugs but also opens avenues for innovative research in medicinal chemistry.

Numéro CAS 
205445-54-1
Formule moléculaire
C 14 H 16 F 3 NON 4
Poids moléculaire 
319.28
Point de fusion 
94 - 100 ?C
Rotation optique 
[a] D 25 = -28,0 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
205445-54-1
Formule moléculaire
C 14 H 16 F 3 NON 4
Poids moléculaire 
319.28
Point de fusion 
94 - 100 ?C
Rotation optique 
[a] D 25 = -28,0 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-3,4,5-trifluoro-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 the development of pharmaceuticals that target specific biological pathways.
  • Drug Development: Its unique trifluoromethyl group enhances the bioactivity of drug candidates, making it valuable in the design of more effective therapeutic agents.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, helping to elucidate complex biological mechanisms.
  • Fluorinated Amino Acids: It is employed in the creation of fluorinated amino acids, which are important for developing imaging agents in medical diagnostics.
  • Material Science: The compound's properties make it suitable for applications in creating advanced materials, including coatings and polymers with enhanced chemical resistance.

Citations