3-Bromo-2,6-Dimethoxypyridine
98%
- Product Code: 69914
CAS:
13445-16-4
| Molecular Weight: | 218.05 g./mol | Molecular Formula: | C₇H₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08669938 | |
| Melting Point: | Boiling Point: | 223.6°C | |
| Density: | 1.484g/mL | Storage Condition: | room temperature, dry |
Product Description:
3-Bromo-2,6-dimethoxypyridine is primarily used as a versatile intermediate in organic synthesis. It plays a significant role in the development of pharmaceuticals, particularly in the construction of complex molecules. The bromine atom on the pyridine ring makes it a valuable substrate for various cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds. Additionally, its dimethoxy groups can act as directing groups or provide steric and electronic effects, influencing the reactivity and selectivity of the compound. This chemical is also employed in agrochemical research for the synthesis of novel compounds with potential pesticidal or herbicidal properties. Its stability and reactivity make it a useful building block in medicinal chemistry for designing drug candidates targeting specific biological pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $33.22 |
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| 5.000 | 10-20 days | $132.89 |
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| 10.000 | 10-20 days | $248.34 |
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3-Bromo-2,6-Dimethoxypyridine
3-Bromo-2,6-dimethoxypyridine is primarily used as a versatile intermediate in organic synthesis. It plays a significant role in the development of pharmaceuticals, particularly in the construction of complex molecules. The bromine atom on the pyridine ring makes it a valuable substrate for various cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for creating carbon-carbon or carbon-nitrogen bonds. Additionally, its dimethoxy groups can act as directing groups or provide steric and electronic effects, influencing the reactivity and selectivity of the compound. This chemical is also employed in agrochemical research for the synthesis of novel compounds with potential pesticidal or herbicidal properties. Its stability and reactivity make it a useful building block in medicinal chemistry for designing drug candidates targeting specific biological pathways.
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