tert-butyl 3-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
95%
- Product Code: 92552
CAS:
1092563-74-0
| Molecular Weight: | 377.28608 g./mol | Molecular Formula: | C₁₉H₃₂BN₃O₄ |
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| 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 functional group makes it valuable in Suzuki-Miyaura couplings, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular construction is critical. Additionally, its piperidine and pyrazole moieties contribute to its role in designing biologically active compounds, particularly in drug discovery efforts targeting central nervous system disorders and other therapeutic areas. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, ensuring efficient handling and reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $513.51 |
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| 0.025 | 10-20 days | $1,663.49 |
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tert-butyl 3-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functional group makes it valuable in Suzuki-Miyaura couplings, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular construction is critical. Additionally, its piperidine and pyrazole moieties contribute to its role in designing biologically active compounds, particularly in drug discovery efforts targeting central nervous system disorders and other therapeutic areas. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, ensuring efficient handling and reactivity.
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