6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-naphthoic acid
97%
- Product Code: 192481
CAS:
2567498-00-2
| Molecular Weight: | 409.43 g./mol | Molecular Formula: | C₂₆H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34178737 | |
| Melting Point: | Boiling Point: | 630.0±30.0 °C(Predicted) | |
| Density: | 1.365±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in peptide synthesis as a protected amino acid building block. The fluorenylmethyloxycarbonyl (Fmoc) group acts as a protecting group for the amine function, allowing selective deprotection under mild basic conditions while maintaining stability during coupling reactions. Its naphthoic acid structure provides a bulky aromatic framework, useful in promoting solubility in organic solvents and aiding in chromatographic purification. Commonly employed in the synthesis of complex peptides and bioactive molecules where steric hindrance and monitoring of reaction progress (via UV detection) are advantageous. Also utilized in the development of fluorescent probes and labeled peptides due to the inherent fluorescence of the fluorenyl moiety.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿22,550.00 |
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6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-naphthoic acid
Used primarily in peptide synthesis as a protected amino acid building block. The fluorenylmethyloxycarbonyl (Fmoc) group acts as a protecting group for the amine function, allowing selective deprotection under mild basic conditions while maintaining stability during coupling reactions. Its naphthoic acid structure provides a bulky aromatic framework, useful in promoting solubility in organic solvents and aiding in chromatographic purification. Commonly employed in the synthesis of complex peptides and bioactive molecules where steric hindrance and monitoring of reaction progress (via UV detection) are advantageous. Also utilized in the development of fluorescent probes and labeled peptides due to the inherent fluorescence of the fluorenyl moiety.
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