3-Bromo-2-fluoro-5-nitropyridine
97%
- Product Code: 42413
CAS:
1868-58-2
| Molecular Weight: | 220.9840 g./mol | Molecular Formula: | C₅H₂BrFN₂O₂ |
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| EC Number: | MDL Number: | MFCD08703668 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its reactive sites, including the bromo, fluoro, and nitro groups, make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active molecules. Additionally, its nitro group can be reduced to form amines, which are key functional groups in many drug candidates. The compound’s unique substitution pattern also allows for selective functionalization, enabling the creation of tailored compounds for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,404.00 |
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3-Bromo-2-fluoro-5-nitropyridine
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its reactive sites, including the bromo, fluoro, and nitro groups, make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active molecules. Additionally, its nitro group can be reduced to form amines, which are key functional groups in many drug candidates. The compound’s unique substitution pattern also allows for selective functionalization, enabling the creation of tailored compounds for research and industrial applications.
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