1-(3,5-Difluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
95%
- Product Code: 39257
CAS:
1415825-04-5
| Molecular Weight: | 320.14 g./mol | Molecular Formula: | C₁₆H₁₉BF₂N₂O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. The difluorobenzyl moiety enhances its potential in designing bioactive molecules, particularly in the creation of enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity make it suitable for constructing complex molecular frameworks in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $402.39 |
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| 0.250 | 10-20 days | $671.21 |
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| 1.000 | 10-20 days | $1,389.76 |
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1-(3,5-Difluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This compound is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. The difluorobenzyl moiety enhances its potential in designing bioactive molecules, particularly in the creation of enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity make it suitable for constructing complex molecular frameworks in medicinal chemistry research.
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