(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromo-5-fluorophenyl)propanoic acid
95%
- Product Code: 38014
CAS:
2278366-87-1
| Molecular Weight: | 484.31 g./mol | Molecular Formula: | C₂₄H₁₉BrFNO₄ |
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| EC Number: | MDL Number: | ||
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| Density: | 1.495±0.06 g/cm3(Predicted) | Storage Condition: | RT |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromo and fluoro substituents on the phenyl ring make it a valuable building block for introducing specific structural motifs into peptides, particularly in the development of bioactive molecules or pharmaceuticals. Its application is significant in medicinal chemistry for designing peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, the bromine atom can be utilized in further functionalization reactions, such as cross-coupling, to create more complex structures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €498.62 |
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| 0.250 | 10-20 days | €819.16 |
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| 1.000 | 10-20 days | €1,638.32 |
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(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromo-5-fluorophenyl)propanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromo and fluoro substituents on the phenyl ring make it a valuable building block for introducing specific structural motifs into peptides, particularly in the development of bioactive molecules or pharmaceuticals. Its application is significant in medicinal chemistry for designing peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, the bromine atom can be utilized in further functionalization reactions, such as cross-coupling, to create more complex structures.
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