3,4-Dimethoxyphenylboronic acid
97%
- Product Code: 89918
Alias:
3,4-Dimethoxyphenylboronic acid
CAS:
122775-35-3
| Molecular Weight: | 181.98 g./mol | Molecular Formula: | C₈H₁₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01074574 | |
| Melting Point: | 245-250 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
3,4-Dimethoxyphenylboronic 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 production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex organic molecules. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its methoxy substituents enhance its stability and reactivity in various chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97-100 |
| APPEARANCE | White to yellow crystals to 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 | ฿310.00 |
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| 5.000 | 10-20 days | ฿810.00 |
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| 25.000 | 10-20 days | ฿3,860.00 |
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| 100.000 | 10-20 days | ฿14,420.00 |
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3,4-Dimethoxyphenylboronic acid
3,4-Dimethoxyphenylboronic 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 production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex organic molecules. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its methoxy substituents enhance its stability and reactivity in various chemical processes.
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