Fmoc-2,4-difluoro-L-homophenylalanine
95%
- Product Code: 38038
CAS:
1260607-93-9
| Molecular Weight: | 437.4354 g./mol | Molecular Formula: | C₂₅H₂₁F₂NO₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. It is employed to introduce 2,4-difluoro-L-homophenylalanine residues into peptide chains, which can enhance the stability and biological activity of the synthesized peptides. The Fmoc group serves as a protective group for the amino acid during the synthesis process, ensuring selective deprotection and coupling steps. It is especially useful in the development of peptide-based drugs, where specific modifications like fluorination can improve metabolic stability, binding affinity, or other pharmacological properties. Additionally, it finds applications in research focused on studying peptide-protein interactions and designing bioactive peptides with tailored functionalities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | £195.61 |
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Fmoc-2,4-difluoro-L-homophenylalanine
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. It is employed to introduce 2,4-difluoro-L-homophenylalanine residues into peptide chains, which can enhance the stability and biological activity of the synthesized peptides. The Fmoc group serves as a protective group for the amino acid during the synthesis process, ensuring selective deprotection and coupling steps. It is especially useful in the development of peptide-based drugs, where specific modifications like fluorination can improve metabolic stability, binding affinity, or other pharmacological properties. Additionally, it finds applications in research focused on studying peptide-protein interactions and designing bioactive peptides with tailored functionalities.
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