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CAS 175277-67-5

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2,6-Dichloro-4-(trifluoromethyl)-3-pyridinamine

Description:
2,6-Dichloro-4-(trifluoromethyl)-3-pyridinamine is a chemical compound characterized by its pyridine ring structure, which is substituted at the 2 and 6 positions with chlorine atoms and at the 4 position with a trifluoromethyl group. This compound is classified as an aromatic amine due to the presence of an amino group (-NH2) attached to the pyridine ring. The trifluoromethyl group contributes to its lipophilicity and can influence its biological activity, making it of interest in pharmaceutical research. The dichloro substitutions enhance the compound's reactivity and may affect its solubility in various solvents. It is important to handle this compound with care, as many chlorinated and fluorinated compounds can exhibit toxicity or environmental persistence. The compound's unique structure may lead to specific interactions in biological systems, making it a candidate for further studies in medicinal chemistry and agrochemicals. As with any chemical, proper safety protocols should be followed during handling and experimentation.
Formula:C6H3Cl2F3N2
InChI:InChI=1S/C6H3Cl2F3N2/c7-3-1-2(6(9,10)11)4(12)5(8)13-3/h1H,12H2
InChI key:InChIKey=BVJJNBRZQVLPIC-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C(N)=C(Cl)N=C(Cl)C1
Synonyms:
  • 2,6-Dichloro-4-(Trifluoromethyl)Pyridin-3-Amine
  • 2,6-Dichloro-4-(trifluoromethyl)-3-pyridinamine
  • 2,6-Dichloro-4-trifluoromethyl-5-aminopyridine
  • 3-Amino-2,6-dichloro-4-(trifluoromethyl)
  • 3-Pyridinamine, 2,6-dichloro-4-(trifluoromethyl)-
  • 3-[2-oxo-5-(trifluoromethyl)pyridin-1(2H)-yl]propanenitrile
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