2,6-Difluoro-3-methoxyphenylboronic acid
98%
- Product Code: 89902
CAS:
870779-02-5
| Molecular Weight: | 187.94 g./mol | Molecular Formula: | C₇H₇BF₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06657880 | |
| Melting Point: | 112-114°C | Boiling Point: | 332.7°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biaryl compounds. These compounds are often explored for their potential therapeutic properties, including anticancer, antiviral, and anti-inflammatory activities. Additionally, it is used in material science for the development of organic electronic materials, such as polymers and small molecules, which are essential for applications in organic light-emitting diodes (OLEDs) and other advanced technologies. Its fluorine and methoxy substituents enhance its reactivity and selectivity in these processes, making it a valuable reagent in modern chemical research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿315.00 |
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| 1.000 | 10-20 days | ฿468.00 |
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| 5.000 | 10-20 days | ฿2,151.00 |
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2,6-Difluoro-3-methoxyphenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biaryl compounds. These compounds are often explored for their potential therapeutic properties, including anticancer, antiviral, and anti-inflammatory activities. Additionally, it is used in material science for the development of organic electronic materials, such as polymers and small molecules, which are essential for applications in organic light-emitting diodes (OLEDs) and other advanced technologies. Its fluorine and methoxy substituents enhance its reactivity and selectivity in these processes, making it a valuable reagent in modern chemical research and industrial applications.
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