2-Trifluoromethyl-6-(piperidin-4-yl)pyridine-4-boronic acid

95%

Reagent Code: #91789
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CAS Number 2225177-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.0472696 g/mol
Formula C₁₁H₁₄BF₃N₂O₂
inventory_2 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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Size Availability Unit Price Quantity
inventory 5mg
10-20 days £1,973.38
inventory 25mg
10-20 days £5,130.62
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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