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Structure of 1588908-99-9
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This cyclopropyl-substituted benzoic acid features a trifluoromethyl group at the para position, enhancing electron-withdrawal and metabolic stability. The cyclopropyl moiety introduces steric constraint and modulates lipophilicity, making it valuable for medicinal chemistry applications where enhanced membrane permeability and target binding are required.
3-Cyclopropyl-5-(trifluoromethyl)benzoic acid serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical scaffolds. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the cyclopropyl substituent contributes to conformational rigidity. The carboxylic acid functionality facilitates direct derivatization or coupling reactions, offering reliable access to amides, esters, and other key intermediates under standard synthetic conditions.
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Lot numbers can be found on the outside label of a product: