(2-((Dimethylamino)methyl)phenyl)boronic acid
98%
- Product Code: 89659
CAS:
85107-53-5
| Molecular Weight: | 179.02 g./mol | Molecular Formula: | C₉H₁₄BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318999 | |
| Melting Point: | Boiling Point: | 309.1°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-((Dimethylamino)methyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with boronic acids to create complex organic molecules. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it useful in biochemical and diagnostic applications. Its dimethylamino group further enhances its reactivity and solubility in various solvents, facilitating its use in diverse chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| PURITYLC | 98 100% |
| APPEARANCE | White to off-white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿480.00 |
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| 1.000 | 10-20 days | ฿1,600.00 |
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| 5.000 | 10-20 days | ฿5,660.00 |
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(2-((Dimethylamino)methyl)phenyl)boronic acid
(2-((Dimethylamino)methyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with boronic acids to create complex organic molecules. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it useful in biochemical and diagnostic applications. Its dimethylamino group further enhances its reactivity and solubility in various solvents, facilitating its use in diverse chemical processes.
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