N-(2-Methoxyethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
98%
- Product Code: 214679
CAS:
1073353-64-6
| Molecular Weight: | 305.18 g./mol | Molecular Formula: | C₁₆H₂₄BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09266187 | |
| Melting Point: | 93-98 °C | Boiling Point: | 448.2±30.0 °C(Predicted) |
| Density: | 1.08±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, 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 research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heterobiaryl systems. Its amide functionality provides a handle for further derivatization or incorporation into larger molecular frameworks. Due to the stability and reactivity profile, it is favored in late-stage functionalization during drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $90.94 |
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| 1g | 10-20 days | $226.54 |
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| 5g | 10-20 days | $676.97 |
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N-(2-Methoxyethyl)-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 research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heterobiaryl systems. Its amide functionality provides a handle for further derivatization or incorporation into larger molecular frameworks. Due to the stability and reactivity profile, it is favored in late-stage functionalization during drug discovery.
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