2-[4-(Trifluoromethyl)phenyl]cyclopropanecarboxylic acid, with the CAS number 2262-03-5, is an organic compound characterized by its cyclopropane structure and the presence of a trifluoromethyl group attached to a phenyl ring. This compound typically exhibits properties associated with both aromatic and aliphatic systems, including potential acidity due to the carboxylic acid functional group. The trifluoromethyl group is known for its electron-withdrawing effects, which can influence the compound's reactivity and stability. As a result, this substance may exhibit unique chemical behavior, such as increased lipophilicity and altered solubility in various solvents. Its structural features suggest potential applications in pharmaceuticals or agrochemicals, where the trifluoromethyl group can enhance biological activity or selectivity. Additionally, the cyclopropane moiety may contribute to the compound's conformational rigidity, impacting its interaction with biological targets. Overall, this compound's distinctive characteristics make it of interest in synthetic chemistry and medicinal research.

2-[4-(trifluoromethyl)phenyl]cyclopropanecarboxylic acid

2262-03-5: 2-[4-(Trifluoromethyl)phenyl]cyclopropanecarboxylic acid, with the CAS number 2262-03-5, is an organic compound characterized by its cyclopropane structure and the presence of a trifluoromethyl group attached to a phenyl ring. This compound typically exhibits properties associated with both aromatic and aliphatic systems, including potential acidity due to the carboxylic acid functional group. The trifluoromethyl group is known for its electron-withdrawing effects, which can influence the compound's reactivity and stability. As a result, this substance may exhibit unique chemical behavior, such as increased lipophilicity and altered solubility in various solvents. Its structural features suggest potential applications in pharmaceuticals or agrochemicals, where the trifluoromethyl group can enhance biological activity or selectivity. Additionally, the cyclopropane moiety may contribute to the compound's conformational rigidity, impacting its interaction with biological targets. Overall, this compound's distinctive characteristics make it of interest in synthetic chemistry and medicinal research.

CAS 2262-03-5

2-[4-(trifluoromethyl)phenyl]cyclopropanecarboxylic acid

2-(4-(trifluoroMethyl)phenyl)cyclopropanecarboxylic acid

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