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CAS 1221171-79-4

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2-Chloro-3-(trifluoromethoxy)-4-pyridinamine

Description:
2-Chloro-3-(trifluoromethoxy)-4-pyridinamine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a chloro group at the second position and a trifluoromethoxy group at the third position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents due to the electronegative chlorine and trifluoromethoxy groups, which can influence its polarity. The trifluoromethoxy group imparts significant electron-withdrawing characteristics, potentially enhancing the compound's reactivity in nucleophilic substitution reactions. Additionally, the presence of the amino group at the fourth position can facilitate hydrogen bonding, affecting its interactions in biological systems. Overall, 2-Chloro-3-(trifluoromethoxy)-4-pyridinamine is of interest in medicinal chemistry and material science due to its potential applications in drug development and as a building block in organic synthesis.
Formula:C6H4ClF3N2O
InChI:InChI=1S/C6H4ClF3N2O/c7-5-4(13-6(8,9)10)3(11)1-2-12-5/h1-2H,(H2,11,12)
InChI key:InChIKey=KEEKHPXFDBFESD-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C=1C(N)=CC=NC1Cl
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