1,5-Difluoro-3-iodo-2-nitrobenzene
≥95%
- Product Code: 114223
CAS:
771-05-1
| Molecular Weight: | 284.99 g./mol | Molecular Formula: | C₆H₂F₂INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28789226 | |
| Melting Point: | Boiling Point: | 279.1°C at 760 mmHg | |
| Density: | 2.162g/cm3 | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. Its unique structure, featuring fluorine, iodine, and nitro groups, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The iodine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The nitro group can be reduced to an amine, providing a pathway for further functionalization. Additionally, the fluorine atoms enhance the stability and bioavailability of the resulting compounds, making it a key intermediate in drug discovery and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,367.00 |
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| 5.000 | 10-20 days | ฿4,725.00 |
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1,5-Difluoro-3-iodo-2-nitrobenzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. Its unique structure, featuring fluorine, iodine, and nitro groups, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The iodine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The nitro group can be reduced to an amine, providing a pathway for further functionalization. Additionally, the fluorine atoms enhance the stability and bioavailability of the resulting compounds, making it a key intermediate in drug discovery and material science applications.
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