6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester
96%
- Product Code: 49910
CAS:
1402666-66-3
| Molecular Weight: | 230.0586 g./mol | Molecular Formula: | C₈H₈BrNO₂ |
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| EC Number: | MDL Number: | MFCD26517010 | |
| 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 more complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine moiety into target compounds. Additionally, it serves as a precursor in the preparation of agrochemicals and fine chemicals, where the pyridine ring plays a crucial role in the biological activity of the final product. Its ester group can also be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $379.56 |
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6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine moiety into target compounds. Additionally, it serves as a precursor in the preparation of agrochemicals and fine chemicals, where the pyridine ring plays a crucial role in the biological activity of the final product. Its ester group can also be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic chemistry.
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