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CAS 187035-79-6

:

ethyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate

Description:
Ethyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features a chloro substituent at the 2-position and a trifluoromethyl group at the 4-position, contributing to its unique reactivity and properties. The ethyl ester functional group at the 5-position enhances its solubility in organic solvents and may influence its biological activity. The presence of the trifluoromethyl group typically imparts increased lipophilicity and can enhance the compound's potency in pharmaceutical applications. Additionally, the chlorine atom can participate in various chemical reactions, making this compound a valuable intermediate in synthetic organic chemistry. Its molecular structure suggests potential applications in agrochemicals or pharmaceuticals, particularly in the development of compounds with specific biological activities. As with many halogenated compounds, safety and handling precautions are essential due to potential toxicity and environmental impact.
Formula:C8H6ClF3N2O2
InChI:InChI=1/C8H6ClF3N2O2/c1-2-16-6(15)4-3-13-7(9)14-5(4)8(10,11)12/h3H,2H2,1H3
SMILES:CCOC(=O)c1cnc(Cl)nc1C(F)(F)F
Synonyms:
  • Ethyl 2-chloro-4-(trifluoromethyl)pyrimidine-
  • 5-Pyrimidinecarboxylic acid, 2-chloro-4-(trifluoromethyl)-, ethyl ester
  • Ethyl 2-chloro-4-(trifluoromethyl)pyrimidne-5-carboxylate
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