Ethyl 5-bromo-3-methylpicolinate
99%
- Product Code: 120163
CAS:
794592-13-5
| Molecular Weight: | 244.09 g./mol | Molecular Formula: | C₉H₁₀BrNO₂ |
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| EC Number: | MDL Number: | MFCD15523779 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
Ethyl 5-bromo-3-methylpicolinate is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in medicinal chemistry for building diverse molecular architectures. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its ester group also provides versatility, enabling hydrolysis or transesterification to modify the compound for specific applications. Overall, it plays a significant role in advancing drug discovery and agricultural innovation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿576.00 |
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| 5.000 | 10-20 days | ฿2,214.00 |
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| 10.000 | 10-20 days | ฿3,852.00 |
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| 25.000 | 10-20 days | ฿8,820.00 |
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Ethyl 5-bromo-3-methylpicolinate
Ethyl 5-bromo-3-methylpicolinate is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in medicinal chemistry for building diverse molecular architectures. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its ester group also provides versatility, enabling hydrolysis or transesterification to modify the compound for specific applications. Overall, it plays a significant role in advancing drug discovery and agricultural innovation.
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