Fmoc-(S)-3-Amino-4-(4-Trifluoromethyl-phenyl)-butyric acid
98%
- Product Code: 104990
CAS:
270065-81-1
| Molecular Weight: | 469.45 g./mol | Molecular Formula: | C₂₆H₂₂F₃NO₄ |
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| EC Number: | MDL Number: | MFCD01861071 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for incorporating specific amino acid sequences into peptides. The Fmoc group acts as a protecting group for the amine functionality, allowing controlled deprotection during the synthesis process. Its trifluoromethylphenyl moiety contributes to the hydrophobicity and stability of the resulting peptides, making it valuable in designing peptides with specific structural and functional properties. It is commonly applied in pharmaceutical research for developing peptide-based drugs, as well as in biochemical studies to explore protein interactions and enzyme mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,330.00 |
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| 0.250 | 10-20 days | ฿4,941.00 |
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| 1.000 | 10-20 days | ฿12,303.00 |
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Fmoc-(S)-3-Amino-4-(4-Trifluoromethyl-phenyl)-butyric acid
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for incorporating specific amino acid sequences into peptides. The Fmoc group acts as a protecting group for the amine functionality, allowing controlled deprotection during the synthesis process. Its trifluoromethylphenyl moiety contributes to the hydrophobicity and stability of the resulting peptides, making it valuable in designing peptides with specific structural and functional properties. It is commonly applied in pharmaceutical research for developing peptide-based drugs, as well as in biochemical studies to explore protein interactions and enzyme mechanisms.
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