5-Methyl-6-trifluoromethylpyridine-3-boronic acid
95%
- Product Code: 58833
CAS:
1889221-03-7
| Molecular Weight: | 204.9421896 g./mol | Molecular Formula: | C₇H₇BF₃NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
5-Methyl-6-trifluoromethylpyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the development of drugs and bioactive compounds. Additionally, its trifluoromethyl group enhances the stability and reactivity of the resulting products, which is beneficial in medicinal chemistry for improving drug efficacy and metabolic stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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5-Methyl-6-trifluoromethylpyridine-3-boronic acid
5-Methyl-6-trifluoromethylpyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the development of drugs and bioactive compounds. Additionally, its trifluoromethyl group enhances the stability and reactivity of the resulting products, which is beneficial in medicinal chemistry for improving drug efficacy and metabolic stability.
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