tert-Butyl 4-hydroxy-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)piperidine-1-carboxylate
98%
- Product Code: 140976
CAS:
877399-39-8
| Molecular Weight: | 407.3121 g./mol | Molecular Formula: | C₂₀H₃₄BN₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22628001 | |
| Melting Point: | Boiling Point: | 532.5±40.0 °C(Predicted) | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds for pharmaceutical and agrochemical research. The boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in drug discovery for building nitrogen-rich heterocyclic frameworks. Its protected piperidine and hydroxy groups allow further functionalization, enhancing versatility in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $394.98 |
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| 1g | 10-20 days | $1,748.38 |
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tert-Butyl 4-hydroxy-4-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)piperidine-1-carboxylate
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds for pharmaceutical and agrochemical research. The boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in drug discovery for building nitrogen-rich heterocyclic frameworks. Its protected piperidine and hydroxy groups allow further functionalization, enhancing versatility in medicinal chemistry.
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