2-Trifluoromethyl-6-(piperidin-4-yl)pyridine-4-boronic acid
95%
Reagent
Code: #91789
CAS Number
2225177-56-8
blur_circular Chemical Specifications
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Molecular Information
Weight
274.0472696 g/mol
Formula
C₁₁H₁₄BF₃N₂O₂
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Storage & Handling
Storage
-20℃, sealed and dry
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The trifluoromethyl group enhances the compound's stability and can influence the biological activity of the final products. Additionally, the piperidine moiety contributes to the compound's versatility in drug discovery, as it is a common structural motif in bioactive molecules. Its application extends to the development of new materials and ligands for catalysis, where its unique structure can improve reaction efficiency and selectivity.
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2-Trifluoromethyl-6-(piperidin-4-yl)pyridine-4-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The trifluoromethyl group enhances the compound's stability and can influence the biological activity of the final products. Additionally, the piperidine moiety contributes to the compound's versatility in drug discovery, as it is a common structural motif in bioactive molecules. Its application extends to the development of new materials and ligands for catalysis, where its unique structure can improve reaction efficiency and selectivity.
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