N-(4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
98%
- Product Code: 215640
CAS:
1172115-34-2
| Molecular Weight: | 275.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22493971 | |
| Melting Point: | Boiling Point: | 436.9±38.0 °C(Predicted) | |
| Density: | 1.06±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The acetamide functionality provides stability and can act as a directing or protecting group during synthesis. It is especially useful in constructing biaryl structures found in bioactive compounds and functional materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,770.00 |
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| 250mg | 10-20 days | ฿2,980.00 |
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| 1g | 10-20 days | ฿7,990.00 |
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N-(4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The acetamide functionality provides stability and can act as a directing or protecting group during synthesis. It is especially useful in constructing biaryl structures found in bioactive compounds and functional materials.
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