(3-cyclopropyl-5-fluorophenyl)boronic acid
95%
- Product Code: 58198
CAS:
2225181-55-3
Molecular Weight: | 179.9839032 g./mol | Molecular Formula: | C₉H₁₀BFO₂ |
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Density: | Storage Condition: | -20℃ |
Product Description:
(3-cyclopropyl-5-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex molecules, especially those containing cyclopropyl and fluorine substituents, which are often sought after for their unique chemical and biological properties. Its boronic acid group facilitates efficient coupling with various aryl halides, enabling the creation of diverse aromatic structures. Additionally, the presence of the cyclopropyl group can enhance the stability and reactivity of the resulting compounds, making it useful in drug discovery and development.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | ฿16,092.00 |
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0.025 | 10-20 days | ฿32,292.00 |
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(3-cyclopropyl-5-fluorophenyl)boronic acid
(3-cyclopropyl-5-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex molecules, especially those containing cyclopropyl and fluorine substituents, which are often sought after for their unique chemical and biological properties. Its boronic acid group facilitates efficient coupling with various aryl halides, enabling the creation of diverse aromatic structures. Additionally, the presence of the cyclopropyl group can enhance the stability and reactivity of the resulting compounds, making it useful in drug discovery and development.
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