N-Cyclohexyl-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
- Product Code: 215864
CAS:
2828443-89-4
| Molecular Weight: | 343.27 g./mol | Molecular Formula: | C₂₀H₃₀BNO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 483.0±28.0 °C(Predicted) | |
| Density: | 1.07±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
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 research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides structural stability and polarity, making it valuable for constructing bioactive molecules and functional materials. Due to its well-defined reactivity, it is often employed in late-stage functionalization during drug discovery and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,880.00 |
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| 250mg | 10-20 days | ฿3,180.00 |
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| 1g | 10-20 days | ฿8,580.00 |
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N-Cyclohexyl-N-methyl-4-(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 research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides structural stability and polarity, making it valuable for constructing bioactive molecules and functional materials. Due to its well-defined reactivity, it is often employed in late-stage functionalization during drug discovery and development.
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