4-(Dimethylamino)phenylboronic acid
95%
- Product Code: 90531
Alias:
4-(Dimethylamino)phenylboronic acid 4-(N,N-Dimethylamino)phenylboronic acid
CAS:
28611-39-4
| Molecular Weight: | 165 g./mol | Molecular Formula: | C₈H₁₂BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01074642 | |
| Melting Point: | 227 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of sensors and molecular probes due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its dimethylamino group further enhances its utility by improving solubility and reactivity in various organic solvents.
Product Specification:
| Test | Specification |
|---|---|
| PURITYLC | 94.5-105.5 |
| APPEARANCE | POWDER AND/OR CHUNKS |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $125.84 |
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| 5.000 | 10-20 days | $459.33 |
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| 25.000 | 10-20 days | $1,482.98 |
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4-(Dimethylamino)phenylboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of sensors and molecular probes due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its dimethylamino group further enhances its utility by improving solubility and reactivity in various organic solvents.
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