3-Cyclopentyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanenitrile
97%
- Product Code: 45405
CAS:
1153949-38-2
| Molecular Weight: | 315.2182 g./mol | Molecular Formula: | C₁₇H₂₆BN₃O₂ |
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| EC Number: | MDL Number: | MFCD18206946 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables it to participate in Suzuki-Miyaura reactions, facilitating the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and advanced materials. Additionally, it is employed in the synthesis of complex molecules, including bioactive compounds and agrochemicals, due to its stability and reactivity under various conditions. Its nitrile group further enhances its versatility, allowing for additional functionalization in synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £13.23 |
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3-Cyclopentyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanenitrile
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables it to participate in Suzuki-Miyaura reactions, facilitating the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and advanced materials. Additionally, it is employed in the synthesis of complex molecules, including bioactive compounds and agrochemicals, due to its stability and reactivity under various conditions. Its nitrile group further enhances its versatility, allowing for additional functionalization in synthetic pathways.
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