(2,6-Difluoro-3-nitrophenyl)boronic acid
95%
- Product Code: 79075
CAS:
1150114-28-5
| Molecular Weight: | 202.91 g./mol | Molecular Formula: | C₆H₄BF₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12025957 | |
| Melting Point: | Boiling Point: | 371.0±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(2,6-Difluoro-3-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules used in pharmaceuticals, agrochemicals, and materials science. The compound's boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with organoboron reagents. Its specific structure, featuring fluorine and nitro groups, enhances its reactivity and selectivity in these transformations. Additionally, it finds applications in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it valuable in biochemical research and diagnostics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $48.87 |
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| 1.000 | 10-20 days | $121.78 |
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| 5.000 | 10-20 days | $389.38 |
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| 10.000 | 10-20 days | $661.57 |
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(2,6-Difluoro-3-nitrophenyl)boronic acid
(2,6-Difluoro-3-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules used in pharmaceuticals, agrochemicals, and materials science. The compound's boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with organoboron reagents. Its specific structure, featuring fluorine and nitro groups, enhances its reactivity and selectivity in these transformations. Additionally, it finds applications in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it valuable in biochemical research and diagnostics.
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