Methyl 3-bromo-5-fluoropicolinate
96%
- Product Code: 45268
CAS:
1214337-00-4
| Molecular Weight: | 234.0200 g./mol | Molecular Formula: | C₇H₅BrFNO₂ |
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| EC Number: | MDL Number: | MFCD14698117 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
Methyl 3-bromo-5-fluoropicolinate is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for constructing complex molecules. In medicinal chemistry, it is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of halogen atoms can enhance biological activity or improve metabolic stability. Additionally, it serves as a precursor in the preparation of heterocyclic compounds, which are crucial in the design of drugs targeting various diseases. In agrochemical research, this compound is utilized to create novel pesticides or herbicides, leveraging its reactivity to develop potent and selective agents. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, further expands its utility in creating diverse chemical entities for industrial and research applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $162.21 |
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Methyl 3-bromo-5-fluoropicolinate
Methyl 3-bromo-5-fluoropicolinate is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for constructing complex molecules. In medicinal chemistry, it is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of halogen atoms can enhance biological activity or improve metabolic stability. Additionally, it serves as a precursor in the preparation of heterocyclic compounds, which are crucial in the design of drugs targeting various diseases. In agrochemical research, this compound is utilized to create novel pesticides or herbicides, leveraging its reactivity to develop potent and selective agents. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, further expands its utility in creating diverse chemical entities for industrial and research applications.
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