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

95%

  • Product Code: 91789
  CAS:    2225177-56-8
Molecular Weight: 274.0472696 g./mol Molecular Formula: C₁₁H₁₄BF₃N₂O₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: -20℃, sealed and dry
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.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days ฿86,080.00
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-
0.025 10-20 days ฿223,800.00
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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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