1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine
97%
- Product Code: 242702
CAS:
852227-97-5
| Molecular Weight: | 287.20 g./mol | Molecular Formula: | C₁₇H₂₆BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368528 | |
| Melting Point: | 156 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The piperidine moiety contributes to enhanced solubility and biological activity in final compounds, often found in active pharmaceutical ingredients (APIs) targeting central nervous system disorders and other therapeutic areas.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €32.26 |
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| 1.000 | 10-20 days | €86.99 |
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| 5.000 | 10-20 days | €378.11 |
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1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The piperidine moiety contributes to enhanced solubility and biological activity in final compounds, often found in active pharmaceutical ingredients (APIs) targeting central nervous system disorders and other therapeutic areas.
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