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Catalog Number:
33591
CAS Number:
1032337-49-7
Fmoc-2,4-difluoro-L-phénylalanine
Purity:
≥ 97,5 % (HPLC)
Synonym(s):
Fmoc-L-Phe(2,4-DiF)-OH, Acide Fmoc-( S )-2-amino-3-(2,4-difluorophényl)propionique, Fmoc-Phe(2,4-DiF)-OH
Documents
$41.76 /100 mg
Taille
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Product Information

Fmoc-2,4-difluoro-L-phenylalanine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its ability to introduce fluorine atoms into peptide structures, which can enhance the biological activity and stability of the resulting compounds. The Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during synthesis, making it an essential tool for researchers focused on developing novel therapeutics.

With its unique fluorinated structure, Fmoc-2,4-difluoro-L-phenylalanine is ideal for applications in the design of peptide-based drugs, particularly in targeting specific biological pathways or enhancing pharmacokinetic properties. Its use in solid-phase peptide synthesis (SPPS) streamlines the process of creating complex peptides, which are vital in various research areas, including cancer therapy and neurobiology. Researchers can leverage this compound to explore new therapeutic avenues and improve existing peptide drugs, making it a valuable addition to any laboratory focused on peptide chemistry.

Synonyms
Fmoc-L-Phe(2,4-DiF)-OH, Acide Fmoc-( S )-2-amino-3-(2,4-difluorophényl)propionique, Fmoc-Phe(2,4-DiF)-OH
CAS Number
1032337-49-7
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 24 H 19 F 2 NON 4
Molecular Weight
423.41
MDL Number
MFCD07371998
PubChem ID
16244020
Melting Point
153 - 155 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Fmoc-L-Phe(2,4-DiF)-OH, Acide Fmoc-( S )-2-amino-3-(2,4-difluorophényl)propionique, Fmoc-Phe(2,4-DiF)-OH
CAS Number
1032337-49-7
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 24 H 19 F 2 NON 4
Molecular Weight
423.41
MDL Number
MFCD07371998
PubChem ID
16244020
Melting Point
153 - 155 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D
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

Fmoc-2,4-difluoro-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the incorporation of fluorinated amino acids which can enhance the stability and bioactivity of the resulting peptides.
  • Drug Development: Its unique properties make it valuable in the design of pharmaceuticals, especially in creating compounds with improved pharmacokinetics and selectivity, which is essential in the development of targeted therapies.
  • Bioconjugation: The presence of the Fmoc protecting group allows for selective reactions in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is important in creating targeted drug delivery systems.
  • Research in Protein Engineering: Researchers utilize this amino acid to study protein folding and stability, as the difluoro substitution can significantly influence the structural properties of proteins, leading to insights in protein design.
  • Fluorine Chemistry Studies: The incorporation of fluorine into organic compounds is a growing field, and this amino acid serves as a model compound for studying the effects of fluorination on biological activity and chemical reactivity.

Citations