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CAS 672-42-4

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2-Trifluoromethyl-4-aminopyrimidine

Description:
2-Trifluoromethyl-4-aminopyrimidine is a heterocyclic organic compound characterized by the presence of a pyrimidine ring substituted with a trifluoromethyl group and an amino group. The trifluoromethyl group (-CF3) is known for its electron-withdrawing properties, which can significantly influence the compound's reactivity and stability. The amino group (-NH2) contributes to the compound's basicity and potential for forming hydrogen bonds, making it useful in various chemical reactions and applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its unique structure allows it to participate in diverse chemical transformations, making it of interest in medicinal chemistry and material science. Additionally, the presence of fluorine atoms can enhance the lipophilicity and metabolic stability of derivatives, which is advantageous in drug design. Overall, 2-Trifluoromethyl-4-aminopyrimidine serves as a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
Formula:C5H4F3N3
InChI:InChI=1/C5H4F3N3/c6-5(7,8)4-10-2-1-3(9)11-4/h1-2H,(H2,9,10,11)
SMILES:c1cnc(C(F)(F)F)[nH]c1=N
Synonyms:
  • 2-(Trifluoromethyl)-4-pyrimidinamine
  • 2-Trifluoromethylpyrimidin-4-ylamine
  • 2-(Trifluoromethyl)Pyrimidin-4-Amine
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