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Structure of 2007426-87-9
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This difluorinated acetic acid derivative features a thiazol-5-yl group that enhances electron-withdrawing character and metabolic stability. The geminal difluoro substitution imparts strong polarity and resistance to enzymatic degradation, making it valuable for synthesizing bioactive molecules in medicinal chemistry and agrochemical research.
2,2-Difluoro-2-(thiazol-5-yl)acetic acid serves as a valuable building block in medicinal chemistry, enabling the construction of fluorinated heterocyclic scaffolds. Its difluoromethyl group imparts enhanced metabolic stability and modulates lipophilicity, while the thiazole moiety provides a versatile handle for further derivatization. The compound exhibits good bench stability and facilitates efficient coupling reactions, making it well-suited for use in the synthesis of bioactive molecules and API intermediates.
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Lot numbers can be found on the outside label of a product: