2-Amino-3-(7-fluoro-1H-indol-3-yl)propanoic acid
97%
- Product Code: 42582
CAS:
53314-95-7
| Molecular Weight: | 222.22 g./mol | Molecular Formula: | C₁₁H₁₁FN₂O₂ |
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| EC Number: | MDL Number: | MFCD09264339 | |
| Melting Point: | Boiling Point: | 450.7±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural features, including the indole and fluorine components, make it valuable for designing compounds that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is explored in the development of radiolabeled probes for imaging studies, aiding in the understanding of brain function and disease mechanisms. Its applications also extend to research in peptide chemistry, where it is incorporated into peptide chains to study structure-activity relationships and enhance therapeutic efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $259.39 |
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| 0.250 | 10-20 days | $518.78 |
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2-Amino-3-(7-fluoro-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural features, including the indole and fluorine components, make it valuable for designing compounds that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is explored in the development of radiolabeled probes for imaging studies, aiding in the understanding of brain function and disease mechanisms. Its applications also extend to research in peptide chemistry, where it is incorporated into peptide chains to study structure-activity relationships and enhance therapeutic efficacy.
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