(3-Methoxy-2-methylphenyl)boronic acid
97%
- Product Code: 118158
CAS:
1313617-76-3
| Molecular Weight: | 165.98 g./mol | Molecular Formula: | C₈H₁₁BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18398348 | |
| Melting Point: | Boiling Point: | 325.8±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
(3-Methoxy-2-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. 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 valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,152.00 |
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| 0.250 | 10-20 days | ฿1,998.00 |
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| 1.000 | 10-20 days | ฿6,480.00 |
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(3-Methoxy-2-methylphenyl)boronic acid
(3-Methoxy-2-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. 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 valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.
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