N-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
- Product Code: 215641
CAS:
1036990-35-8
| Molecular Weight: | 289.18 g./mol | Molecular Formula: | C₁₆H₂₄BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22493990 | |
| Melting Point: | Boiling Point: | 423.9±28.0 °C(Predicted) | |
| Density: | 1.05±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl systems. Its amide functionality allows for further derivatization or integration into larger molecular frameworks, enhancing its utility in drug discovery and development. The presence of the isopropyl group can influence solubility and reactivity, offering advantages in reaction optimization and selectivity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,130.00 |
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| 1.000 | 10-20 days | ฿11,000.00 |
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| 5.000 | 10-20 days | ฿39,600.00 |
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N-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl systems. Its amide functionality allows for further derivatization or integration into larger molecular frameworks, enhancing its utility in drug discovery and development. The presence of the isopropyl group can influence solubility and reactivity, offering advantages in reaction optimization and selectivity.
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