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Catalog Number:
05113
CAS Number:
117666-94-1
Boc-4-benzoyl-D-phénylalanine
Purity:
≥ 99%
Synonym(s):
Boc-D-Bpa-OH, Boc-D-Phe(4-Bz)-OH
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Informations sur le produit

Boc-4-benzoyl-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and proteins. Its unique structure, characterized by the presence of a benzoyl group, allows for selective reactions, facilitating the synthesis of bioactive compounds with potential therapeutic applications.

In the pharmaceutical industry, Boc-4-benzoyl-D-phenylalanine serves as a crucial building block in the design of peptide-based drugs, particularly those targeting specific receptors or enzymes. Its ability to improve the pharmacokinetic properties of peptides makes it a valuable asset in drug development. Additionally, this compound is instrumental in the study of protein interactions and enzyme mechanisms, providing researchers with essential insights into biological processes. With its robust applications and significant advantages over similar compounds, Boc-4-benzoyl-D-phenylalanine stands out as a key ingredient for innovative research and development in biochemistry and medicinal chemistry.

Numéro CAS 
117666-94-1
Formule moléculaire
C 21 H 235
Poids moléculaire 
369.4
Point de fusion 
91 - 92 °C
Rotation optique 
[a] 20 D = -17 ± 1 ° (C=1 dans EtOH)
Informations générales
Numéro CAS 
117666-94-1
Formule moléculaire
C 21 H 235
Poids moléculaire 
369.4
Point de fusion 
91 - 92 °C
Rotation optique 
[a] 20 D = -17 ± 1 ° (C=1 dans EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-4-benzoyl-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a role in the design of novel drug candidates, particularly in the field of cancer research, by modifying the structure of bioactive peptides to enhance their efficacy and stability.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules, improving the delivery and targeting of therapeutic agents.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter functions, aiding researchers in understanding the mechanisms of action of various neuroactive compounds.
  • Cosmetic Formulations: The compound finds applications in cosmetic chemistry, where it can be used to enhance the stability and effectiveness of active ingredients in skin care products.

Citations