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Structure of 53985-49-2
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3-Chloro-5-(trifluoromethyl)benzoic acid features a trifluoromethyl group that enhances electron-withdrawal and metabolic stability, while the ortho-chloro substituent provides steric and electronic modulation. This combination delivers robust functionality in medicinal chemistry applications, particularly as a building block for bioactive molecules requiring lipophilic character and resistance to oxidative degradation.
3-Chloro-5-(trifluoromethyl)benzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization via standard carboxylic acid transformations. Its electron-withdrawing trifluoromethyl and chloro substituents enhance metabolic stability and modulate electronic properties, while the carboxylic acid group facilitates amide coupling, esterification, and salt formation. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for scalable synthesis workflows.
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Lot numbers can be found on the outside label of a product: