4-Fluoro-2-(iso-propyl)pyridine-5-boronic acid
95%
- Product Code: 92161
CAS:
2225174-82-1
| Molecular Weight: | 182.9878432 g./mol | Molecular Formula: | C₈H₁₁BFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed as a building block for creating heterocyclic compounds, which are essential in drug discovery and development. Additionally, its fluorine substituent can enhance the biological activity and metabolic stability of the resulting compounds, making it a useful intermediate in medicinal chemistry. The iso-propyl group further contributes to the steric and electronic properties, influencing the reactivity and selectivity of the molecule in various synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $413.71 |
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| 0.025 | 10-20 days | $1,772.03 |
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| 0.100 | 10-20 days | $5,316.88 |
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4-Fluoro-2-(iso-propyl)pyridine-5-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed as a building block for creating heterocyclic compounds, which are essential in drug discovery and development. Additionally, its fluorine substituent can enhance the biological activity and metabolic stability of the resulting compounds, making it a useful intermediate in medicinal chemistry. The iso-propyl group further contributes to the steric and electronic properties, influencing the reactivity and selectivity of the molecule in various synthetic pathways.
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