2-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid
95%
- Product Code: 59429
CAS:
2225172-49-4
| Molecular Weight: | 205.9814232 g./mol | Molecular Formula: | C₉H₈BFN₂O₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
2-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key reagent, enabling the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Its specific structure, featuring a fluorine atom and a pyrazole moiety, enhances its reactivity and selectivity in these reactions, making it useful for synthesizing complex molecules. Additionally, it may find applications in the development of bioactive compounds or as an intermediate in the creation of functionalized organic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft352,959.78 |
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2-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid
2-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key reagent, enabling the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Its specific structure, featuring a fluorine atom and a pyrazole moiety, enhances its reactivity and selectivity in these reactions, making it useful for synthesizing complex molecules. Additionally, it may find applications in the development of bioactive compounds or as an intermediate in the creation of functionalized organic materials.
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