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CAS 49713-56-6

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4-chloro-6-(trifluoromethyl)quinoline

Description:
4-Chloro-6-(trifluoromethyl)quinoline is a heterocyclic organic compound characterized by a quinoline core structure, which consists of a fused benzene and pyridine ring. The presence of a chloro group at the 4-position and a trifluoromethyl group at the 6-position significantly influences its chemical properties and reactivity. This compound is typically a pale yellow solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. The trifluoromethyl group enhances lipophilicity and metabolic stability, making it an attractive scaffold in drug design. Additionally, the chlorine substituent can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound's molecular structure contributes to its unique electronic properties, which can affect its interaction with biological targets. As with many fluorinated compounds, it may exhibit increased resistance to degradation, impacting its environmental behavior. Safety data should be consulted for handling and exposure guidelines, as halogenated compounds can pose health risks.
Formula:C3H5F2NO
InChI:InChI=1/C3H5F2NO/c1-3(4,5)2(6)7/h1H3,(H2,6,7)
SMILES:CC(C(=N)O)(F)F
Synonyms:
  • 2,2-Difluoropropanamide
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