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CAS 215654-84-5

:

ethyl 1-[4-(trifluoromethyl)pyrimidin-2-yl]piperidine-4-carboxylate

Description:
Ethyl 1-[4-(trifluoromethyl)pyrimidin-2-yl]piperidine-4-carboxylate is a chemical compound characterized by its complex structure, which includes a piperidine ring, a pyrimidine moiety, and a trifluoromethyl group. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The ethyl ester functional group contributes to its solubility properties and reactivity, potentially allowing for further chemical modifications. This compound is typically synthesized through multi-step organic reactions, which may involve the formation of the piperidine and pyrimidine rings, followed by esterification. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. Additionally, the presence of fluorine atoms often correlates with increased metabolic stability and altered pharmacokinetics. As with many compounds containing heterocycles and fluorinated groups, careful consideration of its safety, toxicity, and environmental impact is essential in its application and handling.
Formula:C13H16F3N3O2
InChI:InChI=1/C13H16F3N3O2/c1-2-21-11(20)9-4-7-19(8-5-9)12-17-6-3-10(18-12)13(14,15)16/h3,6,9H,2,4-5,7-8H2,1H3
SMILES:CCOC(=O)C1CCN(CC1)c1nccc(C(F)(F)F)n1
Synonyms:
  • 4-Piperidinecarboxylic Acid, 1-[4-(Trifluoromethyl)-2-Pyrimidinyl]-, Ethyl Ester
  • Ethyl 1-(4-trifluoromethylpyrimidin-2-yl)piperidine-4-carboxylate
  • ethyl 1-[4-(trifluoromethyl)pyrimidin-2-yl]piperidine-4-carboxylate
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