1-(2,2-difluoroethyl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
95%
- Product Code: 39129
CAS:
1049730-40-6
| Molecular Weight: | 258.0726864 g./mol | Molecular Formula: | C₁₁H₁₇BF₂N₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 333.0±42.0 ℃ at 760 mmHg | |
| Density: | 1.17±0.1 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable for cross-coupling reactions, such as Suzuki-Miyaura reactions, which are essential for forming carbon-carbon bonds. The difluoroethyl group enhances its stability and reactivity, making it suitable for creating complex molecules with potential biological activity. Additionally, it is employed in the synthesis of boron-containing compounds, which are increasingly important in drug discovery and material science due to their unique properties and applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿13,734.00 |
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| 1.000 | 10-20 days | ฿21,033.00 |
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1-(2,2-difluoroethyl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable for cross-coupling reactions, such as Suzuki-Miyaura reactions, which are essential for forming carbon-carbon bonds. The difluoroethyl group enhances its stability and reactivity, making it suitable for creating complex molecules with potential biological activity. Additionally, it is employed in the synthesis of boron-containing compounds, which are increasingly important in drug discovery and material science due to their unique properties and applications.
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