(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromopyridin-2-yl)propanoic acid
95%
- Product Code: 38028
CAS:
282734-37-6
| Molecular Weight: | 467.31 g./mol | Molecular Formula: | C₂₃H₁₉BrN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11615774 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromopyridinyl moiety can act as a reactive handle for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, bioconjugates, or probes. Its application is particularly relevant in medicinal chemistry and biochemical research, where precise control over peptide sequences and modifications is essential. Additionally, the bromine atom can facilitate cross-coupling reactions, enabling the introduction of diverse chemical groups for advanced structural modifications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿12,717.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromopyridin-2-yl)propanoic acid
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromopyridinyl moiety can act as a reactive handle for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, bioconjugates, or probes. Its application is particularly relevant in medicinal chemistry and biochemical research, where precise control over peptide sequences and modifications is essential. Additionally, the bromine atom can facilitate cross-coupling reactions, enabling the introduction of diverse chemical groups for advanced structural modifications.
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