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Catalog Number:
33609
CAS Number:
1217700-70-3
Fmoc-4-fluoro-2-metil-L-fenilalanina
Synonym(s):
Fmoc-L-Phe(4-F,2-CH3)-OH, (Ácido S -Fmoc-2-amino-4-fluoro-2-metilfenilpropiónico, Fmoc-Phe(4-F,2-CH3)-OH
Documents
$79.22 /100 mg
Tamaño
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Product Information

Fmoc-4-fluoro-2-methyl-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a fluorine atom and a methyl group, enhances its reactivity and stability, making it an excellent choice for researchers looking to develop novel peptides with improved pharmacological properties.

In the pharmaceutical industry, Fmoc-4-fluoro-2-methyl-L-phenylalanine is particularly valuable for the synthesis of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the development of targeted drug delivery systems and the creation of biologically active compounds. Researchers appreciate its ability to facilitate the introduction of fluorinated residues, which can significantly influence the biological activity and metabolic stability of peptides. This compound stands out for its ability to enhance the efficacy of peptide drugs while maintaining a favorable safety profile.

Synonyms
Fmoc-L-Phe(4-F,2-CH3)-OH, (Ácido S -Fmoc-2-amino-4-fluoro-2-metilfenilpropiónico, Fmoc-Phe(4-F,2-CH3)-OH
CAS Number
1217700-70-3
Molecular Formula
C 25 H 22 FNO 4
Molecular Weight
419.45
MDL Number
MFCD12198176
PubChem ID
53398090
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Fmoc-L-Phe(4-F,2-CH3)-OH, (Ácido S -Fmoc-2-amino-4-fluoro-2-metilfenilpropiónico, Fmoc-Phe(4-F,2-CH3)-OH
CAS Number
1217700-70-3
Molecular Formula
C 25 H 22 FNO 4
Molecular Weight
419.45
MDL Number
MFCD12198176
PubChem ID
53398090
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-fluoro-2-methyl-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create custom peptides for various applications in drug development and biotechnology.
  • Drug Discovery: Its unique structure enhances the ability to design and optimize new pharmaceutical compounds, particularly in targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The Fmoc group facilitates the attachment of other molecules, such as fluorescent tags or drug molecules, to peptides, which is crucial for developing targeted therapies and diagnostic tools.
  • Research in Neuroscience: The compound's properties are leveraged in studies related to neurotransmitter systems, providing insights into brain function and potential therapeutic targets for neurological disorders.
  • Protein Engineering: It is used in the modification of proteins to enhance their stability and activity, which is essential for developing biopharmaceuticals and enzyme-based applications.

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