Methyl 3-bromo-6-methoxypicolinate
97%
- Product Code: 45325
CAS:
1214332-49-6
| Molecular Weight: | 246.0500 g./mol | Molecular Formula: | C₈H₈NO₃Br |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14698131 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and methoxy group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine rings into target compounds. Additionally, it serves as a precursor in the synthesis of biologically active molecules, including potential drug candidates for therapeutic applications. Its role in medicinal chemistry research is significant, particularly in the design of compounds targeting specific enzymes or receptors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $148.65 |
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Methyl 3-bromo-6-methoxypicolinate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and methoxy group, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine rings into target compounds. Additionally, it serves as a precursor in the synthesis of biologically active molecules, including potential drug candidates for therapeutic applications. Its role in medicinal chemistry research is significant, particularly in the design of compounds targeting specific enzymes or receptors.
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