(3-Fluoro-4-(trifluoromethoxy)phenyl)boronic acid
97%
- Product Code: 113200
CAS:
187804-79-1
| Molecular Weight: | 223.92 g./mol | Molecular Formula: | C₇H₅BF₄O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368680 | |
| Melting Point: | Boiling Point: | 267.1°C at 760 mmHg | |
| Density: | 1.48g/cm3 | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(3-Fluoro-4-(trifluoromethoxy)phenyl)boronic acid is widely used 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. Its unique structure, featuring fluorine and trifluoromethoxy groups, enhances its reactivity and selectivity in coupling reactions, enabling the synthesis of complex molecules with high precision. Additionally, it is utilized in the development of bioactive compounds and as a building block in medicinal chemistry for creating potential drug candidates. Its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $59.46 |
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| 1.000 | 10-20 days | $148.30 |
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| 5.000 | 10-20 days | $498.34 |
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| 10.000 | 10-20 days | $798.48 |
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(3-Fluoro-4-(trifluoromethoxy)phenyl)boronic acid
(3-Fluoro-4-(trifluoromethoxy)phenyl)boronic acid is widely used 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. Its unique structure, featuring fluorine and trifluoromethoxy groups, enhances its reactivity and selectivity in coupling reactions, enabling the synthesis of complex molecules with high precision. Additionally, it is utilized in the development of bioactive compounds and as a building block in medicinal chemistry for creating potential drug candidates. Its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
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