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Catalog Number:
33628
Boc-α-méthyl-L-3-fluorophénylalanine
Synonym(s):
Boc-α-Me-L-Phe(3-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(3-fluorophényl)propanoïque
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$58.39 /100 mg
Taille
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Product Information

Boc-a-methyl-L-3-fluorophenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing novel peptides and biologically active compounds. Its unique fluorinated phenylalanine structure allows for increased lipophilicity and potential bioactivity, paving the way for innovative therapeutic applications, particularly in the fields of drug design and development.

Researchers and industry professionals can leverage Boc-a-methyl-L-3-fluorophenylalanine in the synthesis of peptide-based drugs, where the incorporation of fluorinated amino acids can significantly influence the pharmacokinetic and pharmacodynamic properties of the resulting compounds. This versatility not only aids in the exploration of new therapeutic avenues but also enhances the efficacy and specificity of drug candidates. With its unique properties, this compound stands out as a crucial building block in the advancement of peptide chemistry and medicinal chemistry.

Synonyms
Boc-α-Me-L-Phe(3-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(3-fluorophényl)propanoïque
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.32
MDL Number
MFCD22887395
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Boc-α-Me-L-Phe(3-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(3-fluorophényl)propanoïque
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.32
MDL Number
MFCD22887395
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-a-methyl-L-3-fluorophenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its unique structure allows for the incorporation of fluorinated amino acids, enhancing the stability and bioactivity of the resulting peptides.
  • Drug Development: Researchers leverage this compound in drug discovery processes, especially in designing inhibitors for specific biological targets. The fluorine atom can improve the pharmacokinetic properties of drug candidates, making them more effective.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules. This application is crucial in creating targeted drug delivery systems that can improve treatment efficacy.
  • Research in Neuroscience: The compound is utilized in studies investigating neurotransmitter systems, as its structural features can mimic natural amino acids, aiding in the understanding of receptor interactions.
  • Analytical Chemistry: Boc-a-methyl-L-3-fluorophenylalanine is employed as a standard in analytical methods, helping researchers quantify and analyze amino acid compositions in various samples, which is essential in both clinical and environmental studies.

Citations