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Structure of 767337-59-7
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3-(Trifluoromethyl)thiophene-2-carboxylic acid features a trifluoromethyl group positioned ortho to the carboxylic acid on a thiophene scaffold, delivering enhanced electron-withdrawing character and metabolic stability. This structural motif enables direct incorporation into bioactive scaffolds, particularly in kinase inhibitors and pharmaceutical intermediates where lipophilicity and target affinity are critical. The molecule exhibits robust bench stability and compatibility with standard coupling protocols.
3-(Trifluoromethyl)thiophene-2-carboxylic acid serves as a versatile building block for bioactive heterocycles, enabling efficient access to thiophene-based pharmaceutical scaffolds. Its trifluoromethyl group enhances metabolic stability and modulates electronic properties, while the carboxylic acid functionality facilitates direct amidation, esterification, or coupling reactions. The compound exhibits excellent bench stability and is compatible with standard synthetic workflows in medicinal chemistry and process development.
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Lot numbers can be found on the outside label of a product: