(3,5-Difluoro-2-methoxyphenyl)boronic acid
96%
- Product Code: 89927
CAS:
737000-76-9
| Molecular Weight: | 187.94 g./mol | Molecular Formula: | C₇H₇BF₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095353 | |
| Melting Point: | Boiling Point: | 339.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(3,5-Difluoro-2-methoxyphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the creation of complex organic molecules. The compound serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. Its unique structure, featuring both fluorine and methoxy groups, allows for precise control over the reactivity and selectivity of the coupling process. Additionally, it is utilized in the development of advanced materials, such as organic semiconductors and polymers, where its boronic acid group facilitates the formation of stable covalent bonds with other functional groups. This makes it a valuable reagent in the design and production of innovative materials with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,116.00 |
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| 1.000 | 10-20 days | ฿3,105.00 |
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| 5.000 | 10-20 days | ฿12,078.00 |
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(3,5-Difluoro-2-methoxyphenyl)boronic acid
(3,5-Difluoro-2-methoxyphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the creation of complex organic molecules. The compound serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. Its unique structure, featuring both fluorine and methoxy groups, allows for precise control over the reactivity and selectivity of the coupling process. Additionally, it is utilized in the development of advanced materials, such as organic semiconductors and polymers, where its boronic acid group facilitates the formation of stable covalent bonds with other functional groups. This makes it a valuable reagent in the design and production of innovative materials with tailored properties.
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