3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
97%
- Product Code: 81002
CAS:
214360-46-0
| Molecular Weight: | 229.08 g./mol | Molecular Formula: | C₁₃H₁₆BNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 78-82°C | Boiling Point: | 341°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a precursor in the development of materials for organic electronics, such as OLEDs and sensors, due to its ability to introduce functional groups into aromatic systems. Its stability and reactivity also make it a preferred choice in medicinal chemistry for creating bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿270.00 |
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| 5.000 | 10-20 days | ฿585.00 |
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| 25.000 | 10-20 days | ฿2,313.00 |
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| 100.000 | 10-20 days | ฿7,695.00 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
This compound is widely used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a precursor in the development of materials for organic electronics, such as OLEDs and sensors, due to its ability to introduce functional groups into aromatic systems. Its stability and reactivity also make it a preferred choice in medicinal chemistry for creating bioactive compounds.
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