Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
33627
Boc-α-méthyl-L-2-fluorophénylalanine
Synonym(s):
Boc-α-Me-L-Phe(2-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(2-fluorophényl)propanoïque
Documents
$58.39 /100 mg
Taille
Request Bulk Quote
Product Information

Boc-a-methyl-L-2-fluorophenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound, known for its unique fluorinated side chain, enhances the biological activity and stability of peptides, making it an essential building block in the development of novel therapeutics. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptide structures with precision.

Researchers and industry professionals appreciate Boc-a-methyl-L-2-fluorophenylalanine for its ability to improve the pharmacokinetic properties of peptides, potentially leading to more effective drug candidates. Its application extends to the design of inhibitors and modulators in various biological pathways, particularly in cancer and neurological research. The incorporation of fluorinated amino acids like this one can also enhance the binding affinity of peptides to their targets, providing a significant advantage over non-fluorinated counterparts.

Synonyms
Boc-α-Me-L-Phe(2-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(2-fluorophényl)propanoïque
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.32
MDL Number
MFCD22887382
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Boc-α-Me-L-Phe(2-F)-OH, Acide boc-( S -2-amino-2-méthyl-3-(2-fluorophényl)propanoïque
Molecular Formula
C 15 H 20 FNO 4
Molecular Weight
297.32
MDL Number
MFCD22887382
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-a-methyl-L-2-fluorophenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in the development of novel therapeutics that target specific biological pathways.
  • Drug Development: Its unique fluorinated structure enhances the pharmacological properties of drug candidates, making it valuable in medicinal chemistry for creating more effective pharmaceuticals.
  • Bioconjugation: The compound can be employed in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their efficacy and targeting capabilities.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is used in studies exploring receptor interactions and the development of neuroactive compounds.
  • Analytical Chemistry: The compound is useful in analytical methods, such as chromatography, for separating and identifying amino acids and related compounds in complex mixtures.

Citations