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CAS 1402664-67-8

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6-Methyl-5-(trifluoromethyl)-3-pyridinamine

Description:
6-Methyl-5-(trifluoromethyl)-3-pyridinamine is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a methyl group at the 6-position and a trifluoromethyl group at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and exhibits moderate solubility in polar solvents due to the electronegative trifluoromethyl group, which can influence its reactivity and interaction with other molecules. The trifluoromethyl group is known for imparting lipophilicity and can enhance the compound's biological activity, making it of interest in pharmaceutical research. Additionally, the amino group at the 3-position can participate in hydrogen bonding, further affecting its chemical behavior. Overall, 6-Methyl-5-(trifluoromethyl)-3-pyridinamine is notable for its potential applications in medicinal chemistry and as a building block in the synthesis of more complex organic molecules.
Formula:C7H7F3N2
InChI:InChI=1S/C7H7F3N2/c1-4-6(7(8,9)10)2-5(11)3-12-4/h2-3H,11H2,1H3
InChI key:InChIKey=JIMDKKGPXBJVGB-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(C)N=CC(N)=C1
Synonyms:
  • 3-Pyridinamine, 6-methyl-5-(trifluoromethyl)-
  • 6-Methyl-5-(trifluoromethyl)-3-pyridinamine
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