4-Chloro-2-fluoro-3-methoxyphenylboronic acid
98%
- Product Code: 90624
CAS:
944129-07-1
| Molecular Weight: | 204.39 g./mol | Molecular Formula: | C₇H₇BClFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD1701574 | |
| Melting Point: | 246-249°C | Boiling Point: | 487.6±40.0°C at 760 mmHg |
| Density: | 1.40±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the production of biologically active compounds, such as drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its unique structure, combining chloro, fluoro, and methoxy substituents, allows for precise modifications in target molecules, enhancing their properties or efficacy. Additionally, it is employed in the development of organic electronic materials, where its boronic acid group facilitates the creation of conjugated systems for use in sensors, OLEDs, or other electronic devices.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,340.00 |
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| 1.000 | 10-20 days | ฿3,510.00 |
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| 5.000 | 10-20 days | ฿10,900.00 |
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4-Chloro-2-fluoro-3-methoxyphenylboronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the production of biologically active compounds, such as drug candidates, due to its ability to introduce specific functional groups into molecular frameworks. Its unique structure, combining chloro, fluoro, and methoxy substituents, allows for precise modifications in target molecules, enhancing their properties or efficacy. Additionally, it is employed in the development of organic electronic materials, where its boronic acid group facilitates the creation of conjugated systems for use in sensors, OLEDs, or other electronic devices.
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