Fmoc-Phe(4-CF3)-OH
≥95%
- Product Code: 50395
CAS:
247113-86-6
| Molecular Weight: | 455.43 g./mol | Molecular Formula: | C₂₅H₂₀F₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00797581 | |
| Melting Point: | 128-138°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the trifluoromethyl (CF3) group on the phenyl ring enhances the hydrophobicity and stability of the peptide, making it useful in the development of peptides with specific structural or functional properties. It is often employed in the synthesis of modified peptides for research in drug discovery, biochemical studies, and the development of peptide-based therapeutics. The CF3 group can also influence the peptide's interaction with biological targets, making it valuable in designing peptides with enhanced binding affinity or selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿729.00 |
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| 1.000 | 10-20 days | ฿1,809.00 |
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| 5.000 | 10-20 days | ฿7,281.00 |
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| 10.000 | 10-20 days | ฿13,311.00 |
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Fmoc-Phe(4-CF3)-OH
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the trifluoromethyl (CF3) group on the phenyl ring enhances the hydrophobicity and stability of the peptide, making it useful in the development of peptides with specific structural or functional properties. It is often employed in the synthesis of modified peptides for research in drug discovery, biochemical studies, and the development of peptide-based therapeutics. The CF3 group can also influence the peptide's interaction with biological targets, making it valuable in designing peptides with enhanced binding affinity or selectivity.
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