2-chloro-3-fluoro-5-iodopyridin-4-amine
95%
- Product Code: 124058
CAS:
1801841-62-2
| Molecular Weight: | 272.45 g./mol | Molecular Formula: | C₅H₃ClFIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 326.6±42.0 °C(Predicted) | |
| Density: | 2.211±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile intermediate in the synthesis of more complex molecules. Its unique halogenated pyridine structure makes it valuable for constructing active pharmaceutical ingredients (APIs) and agrochemicals, particularly those targeting specific biological pathways. In medicinal chemistry, it serves as a building block for developing drugs with potential antibacterial, antiviral, or anticancer properties due to its ability to interact with various enzymes and receptors. In agrochemicals, it is used to create pesticides or herbicides with enhanced efficacy and selectivity. Additionally, its halogen atoms provide reactive sites for further functionalization, enabling the development of diverse derivatives for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿13,221.00 |
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| 1.000 | 10-20 days | ฿36,738.00 |
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2-chloro-3-fluoro-5-iodopyridin-4-amine
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile intermediate in the synthesis of more complex molecules. Its unique halogenated pyridine structure makes it valuable for constructing active pharmaceutical ingredients (APIs) and agrochemicals, particularly those targeting specific biological pathways. In medicinal chemistry, it serves as a building block for developing drugs with potential antibacterial, antiviral, or anticancer properties due to its ability to interact with various enzymes and receptors. In agrochemicals, it is used to create pesticides or herbicides with enhanced efficacy and selectivity. Additionally, its halogen atoms provide reactive sites for further functionalization, enabling the development of diverse derivatives for research and industrial applications.
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