Fmoc-D-Phe(4-F)-OH
≥98%
- Product Code: 105031
CAS:
177966-64-2
| Molecular Weight: | 405.42 g./mol | Molecular Formula: | C₂₄H₂₀FNO₄ |
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| EC Number: | MDL Number: | MFCD00235900 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
Fmoc-D-Phe(4-F)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it suitable for the stepwise assembly of peptides. The presence of the para-fluoro substituent on the phenyl ring enhances the stability and can influence the biological activity of the resulting peptides, making it valuable in the development of peptide-based pharmaceuticals. It is also utilized in the study of peptide-protein interactions and in the design of peptide ligands for therapeutic targets, such as receptors or enzymes. Additionally, its chiral nature (D-configuration) is crucial for creating peptides with specific stereochemical properties, which is essential for mimicking natural peptides or designing novel bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,287.00 |
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| 5.000 | 10-20 days | ฿5,013.00 |
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Fmoc-D-Phe(4-F)-OH
Fmoc-D-Phe(4-F)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it suitable for the stepwise assembly of peptides. The presence of the para-fluoro substituent on the phenyl ring enhances the stability and can influence the biological activity of the resulting peptides, making it valuable in the development of peptide-based pharmaceuticals. It is also utilized in the study of peptide-protein interactions and in the design of peptide ligands for therapeutic targets, such as receptors or enzymes. Additionally, its chiral nature (D-configuration) is crucial for creating peptides with specific stereochemical properties, which is essential for mimicking natural peptides or designing novel bioactive compounds.
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