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Structure of 1039621-73-2
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This pyridyl-substituted difluoroacetic acid features a sterically constrained α,α-difluoro motif paired with a heteroaromatic pyridin-2-yl group, enabling enhanced metabolic stability and improved membrane permeability. The electron-deficient acetic acid moiety integrates readily into bioactive scaffolds for medicinal chemistry applications.
2,2-Difluoro-2-(pyridin-2-yl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the introduction of a strongly electron-withdrawing difluoromethyl group adjacent to a pyridine moiety. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient incorporation into bioactive scaffolds. The molecule functions as a key intermediate in the synthesis of fluorinated heterocycles and pharmaceutical candidates requiring enhanced metabolic stability and membrane permeability.
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Lot numbers can be found on the outside label of a product: