(3-Bromo-2-fluorophenyl)boronic acid
95%
- Product Code: 90227
CAS:
352535-97-8
Molecular Weight: | 218.82 g./mol | Molecular Formula: | C₆H₅BBrFO₂ |
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EC Number: | MDL Number: | ||
Melting Point: | 225-227°C | Boiling Point: | 326.6°C |
Density: | Storage Condition: | 2-8°C |
Product Description:
(3-Bromo-2-fluorophenyl)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. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its ability to react with various aryl halides in the presence of a palladium catalyst. Additionally, it is utilized in the development of bioactive compounds and in research focused on creating new drug candidates. Its unique structure, combining bromo and fluoro substituents, allows for selective reactivity, making it a versatile tool in medicinal chemistry and material science.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿423.00 |
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5.000 | 10-20 days | ฿1,908.00 |
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25.000 | 10-20 days | ฿8,352.00 |
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(3-Bromo-2-fluorophenyl)boronic acid
(3-Bromo-2-fluorophenyl)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. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its ability to react with various aryl halides in the presence of a palladium catalyst. Additionally, it is utilized in the development of bioactive compounds and in research focused on creating new drug candidates. Its unique structure, combining bromo and fluoro substituents, allows for selective reactivity, making it a versatile tool in medicinal chemistry and material science.
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