2-(2-Trifluoromethylphenyl)pyridine-4-boronic acid
95%
- Product Code: 91478
CAS:
2225177-15-9
| Molecular Weight: | 267.0115696 g./mol | Molecular Formula: | C₁₂H₉BF₃NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
2-(2-Trifluoromethylphenyl)pyridine-4-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 boronic acid group acts as a key functional moiety, enabling efficient coupling with aryl halides or triflates. Additionally, the trifluoromethyl group enhances the compound's stability and reactivity, making it suitable for creating complex molecules with specific properties. It is also employed in the development of bioactive compounds and in research focused on drug discovery and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿29,700.00 |
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| 0.100 | 10-20 days | ฿82,800.00 |
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2-(2-Trifluoromethylphenyl)pyridine-4-boronic acid
2-(2-Trifluoromethylphenyl)pyridine-4-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 boronic acid group acts as a key functional moiety, enabling efficient coupling with aryl halides or triflates. Additionally, the trifluoromethyl group enhances the compound's stability and reactivity, making it suitable for creating complex molecules with specific properties. It is also employed in the development of bioactive compounds and in research focused on drug discovery and material science.
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