2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-bromo-1H-indol-3-yl)propanoicacid
98%
- Product Code: 197471
CAS:
753504-16-4
| Molecular Weight: | 505.36 g./mol | Molecular Formula: | C₂₆H₂₁BrN₂O₄ |
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| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in peptide synthesis as a protected amino acid building block, this compound enables the controlled assembly of complex peptides containing tryptophan derivatives. The Fmoc group provides orthogonal protection for the alpha-amino function, allowing stepwise chain elongation under mild basic conditions. The bromine substituent on the indole ring offers a site for further functionalization, such as cross-coupling reactions, enabling the synthesis of modified peptides for drug discovery and biochemical studies. It is particularly valuable in solid-phase peptide synthesis (SPPS) for generating analogs used in pharmaceutical research, including those targeting neurological and oncological pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿22,230.00 |
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| 1g | 10-20 days | ฿57,300.00 |
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2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-bromo-1H-indol-3-yl)propanoicacid
Widely used in peptide synthesis as a protected amino acid building block, this compound enables the controlled assembly of complex peptides containing tryptophan derivatives. The Fmoc group provides orthogonal protection for the alpha-amino function, allowing stepwise chain elongation under mild basic conditions. The bromine substituent on the indole ring offers a site for further functionalization, such as cross-coupling reactions, enabling the synthesis of modified peptides for drug discovery and biochemical studies. It is particularly valuable in solid-phase peptide synthesis (SPPS) for generating analogs used in pharmaceutical research, including those targeting neurological and oncological pathways.
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