6-Chloro-4-fluoro-2-(trifluoromethyl)-1H-benzimidazole is a chemical compound characterized by its unique structural features, which include a benzimidazole core substituted with chlorine, fluorine, and trifluoromethyl groups. This compound typically exhibits a solid state at room temperature and is known for its potential biological activity, making it of interest in pharmaceutical research. The presence of multiple fluorine atoms contributes to its lipophilicity and stability, which can enhance its interaction with biological targets. The chlorine and trifluoromethyl groups can influence the compound's electronic properties and reactivity, potentially affecting its pharmacokinetics and pharmacodynamics. As a heterocyclic compound, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Safety and handling precautions should be observed due to the presence of halogenated substituents, which can pose environmental and health risks. Overall, this compound represents a significant interest in medicinal chemistry and material science due to its diverse applications and unique chemical properties.

6-chloro-4-fluoro-2-(trifluoromethyl)-1H-benzimidazole

89426-95-9: 6-Chloro-4-fluoro-2-(trifluoromethyl)-1H-benzimidazole is a chemical compound characterized by its unique structural features, which include a benzimidazole core substituted with chlorine, fluorine, and trifluoromethyl groups. This compound typically exhibits a solid state at room temperature and is known for its potential biological activity, making it of interest in pharmaceutical research. The presence of multiple fluorine atoms contributes to its lipophilicity and stability, which can enhance its interaction with biological targets. The chlorine and trifluoromethyl groups can influence the compound's electronic properties and reactivity, potentially affecting its pharmacokinetics and pharmacodynamics. As a heterocyclic compound, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Safety and handling precautions should be observed due to the presence of halogenated substituents, which can pose environmental and health risks. Overall, this compound represents a significant interest in medicinal chemistry and material science due to its diverse applications and unique chemical properties.

6-Chloro-4-fluoro -2-(trifluoromethyl)-1H-benzimidazole

CAS 89426-95-9

6-chloro-4-fluoro-2-(trifluoromethyl)-1H-benzimidazole

6-Chloro-4-fluoro -2-(trifluoromethyl)-1H-benzimidazole

Ref: 54-PC501019