(2-Formyl-3-methoxyphenyl)boronic acid
98%
- Product Code: 116963
CAS:
958030-46-1
| Molecular Weight: | 179.97 g./mol | Molecular Formula: | C₈H₉BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01319042 | |
| Melting Point: | Boiling Point: | 408.3±55.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(2-Formyl-3-methoxyphenyl)boronic acid is widely utilized 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. The compound’s boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl groups. Additionally, its formyl and methoxy substituents enhance its reactivity and selectivity in complex molecular constructions. It is also employed 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 research and diagnostic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $106.51 |
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| 1.000 | 10-20 days | $212.61 |
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| 5.000 | 10-20 days | $566.81 |
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(2-Formyl-3-methoxyphenyl)boronic acid
(2-Formyl-3-methoxyphenyl)boronic acid is widely utilized 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. The compound’s boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl groups. Additionally, its formyl and methoxy substituents enhance its reactivity and selectivity in complex molecular constructions. It is also employed 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 research and diagnostic applications.
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