5-Fluoro-4-iodopyridin-3-amine
≥98%
- Product Code: 87578
CAS:
1350475-29-4
| Molecular Weight: | 238 g./mol | Molecular Formula: | C₅H₄FIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21362312 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
5-Fluoro-4-iodopyridin-3-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both fluorine and iodine atoms, makes it a valuable building block for developing molecules with potential biological activity. This compound is often employed in the creation of kinase inhibitors, which are essential in targeting specific enzymes involved in cancer and other diseases. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are widely explored for their therapeutic properties in drug discovery. Its versatility in chemical reactions, such as cross-coupling and substitution, further enhances its application in designing novel drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,811.00 |
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| 0.250 | 10-20 days | ฿14,985.00 |
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| 1.000 | 10-20 days | ฿37,422.00 |
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5-Fluoro-4-iodopyridin-3-amine
5-Fluoro-4-iodopyridin-3-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both fluorine and iodine atoms, makes it a valuable building block for developing molecules with potential biological activity. This compound is often employed in the creation of kinase inhibitors, which are essential in targeting specific enzymes involved in cancer and other diseases. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are widely explored for their therapeutic properties in drug discovery. Its versatility in chemical reactions, such as cross-coupling and substitution, further enhances its application in designing novel drug candidates.
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