Tert-butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)piperidine-1-carboxylate
95%
- Product Code: 242075
CAS:
2223053-62-9
| Molecular Weight: | 377.28278 g./mol | Molecular Formula: | C₂₀H₃₂BNO₅ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of palladium catalysts, making it valuable for constructing complex molecules in pharmaceutical and agrochemical research. The piperidine moiety protected by the Boc group allows for further functionalization in drug discovery pathways, particularly in the development of bioactive compounds with nitrogen-containing ring systems. Its stability and reactivity profile make it suitable for late-stage diversification in medicinal chemistry campaigns.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $1,326.04 |
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| 0.100 | 10-20 days | $4,113.87 |
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Tert-butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)piperidine-1-carboxylate
Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of palladium catalysts, making it valuable for constructing complex molecules in pharmaceutical and agrochemical research. The piperidine moiety protected by the Boc group allows for further functionalization in drug discovery pathways, particularly in the development of bioactive compounds with nitrogen-containing ring systems. Its stability and reactivity profile make it suitable for late-stage diversification in medicinal chemistry campaigns.
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