(6-Bromo-2-ethoxy-3-fluorophenyl)boronic acid
≥95%
- Product Code: 120630
CAS:
1310403-98-5
| Molecular Weight: | 262.87 g./mol | Molecular Formula: | C₈H₉BBrFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12026721 | |
| Melting Point: | Boiling Point: | 380.1±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(6-Bromo-2-ethoxy-3-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex organic molecules, including drug candidates. The compound acts as a key intermediate, enabling the formation of carbon-carbon bonds between aryl halides and boronic acids, which is essential for constructing biologically active compounds. Its specific structure, featuring bromo, ethoxy, and fluoro substituents, makes it valuable for introducing these functional groups into target molecules, enhancing their chemical properties or biological activity. Additionally, it is utilized in material science for the development of organic electronic materials, where precise molecular architecture is crucial for performance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿495.00 |
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| 0.250 | 10-20 days | ฿828.00 |
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| 1.000 | 10-20 days | ฿2,475.00 |
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(6-Bromo-2-ethoxy-3-fluorophenyl)boronic acid
(6-Bromo-2-ethoxy-3-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex organic molecules, including drug candidates. The compound acts as a key intermediate, enabling the formation of carbon-carbon bonds between aryl halides and boronic acids, which is essential for constructing biologically active compounds. Its specific structure, featuring bromo, ethoxy, and fluoro substituents, makes it valuable for introducing these functional groups into target molecules, enhancing their chemical properties or biological activity. Additionally, it is utilized in material science for the development of organic electronic materials, where precise molecular architecture is crucial for performance.
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