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Structure of 261635-83-0
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6-Chloro-2-(trifluoromethyl)nicotinic acid features a trifluoromethyl group at the 2-position and a chlorine substituent at the 6-position of the nicotinic acid scaffold. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, particularly for developing kinase inhibitors and bioactive compounds requiring enhanced metabolic stability and lipophilic character.
6-Chloro-2-(trifluoromethyl)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its electron-deficient pyridine core facilitates nucleophilic aromatic substitution and palladium-catalyzed coupling reactions. The trifluoromethyl group enhances metabolic stability and membrane permeability, while the chloro substituent provides a reliable handle for further functionalization. This compound exhibits excellent bench stability and compatibility with standard purification methods, making it ideal for scalable synthesis workflows.
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Lot numbers can be found on the outside label of a product: