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Structure of 1356999-25-1
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This acetyl derivative features a 2,4-difluoro-6-hydroxyphenyl moiety, offering enhanced solubility and stability in polar solvents. The electron-deficient aryl ring facilitates electrophilic substitution, while the phenolic hydroxyl enables hydrogen bonding and derivatization. This scaffold integrates readily into bioactive molecule design and serves as a key intermediate in pharmaceutical synthesis under standard conditions.
1-(2,4-Difluoro-6-hydroxyphenyl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic hydroxyl group. Its trifluoromethyl-like electronic profile and ortho-fluorine substituents enhance metabolic stability and modulate reactivity in subsequent coupling reactions. The ketone functionality facilitates nucleophilic additions and enolate chemistry, while the bench-stable structure simplifies purification and integration into multi-step syntheses of bioactive heterocycles and API intermediates.
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Lot numbers can be found on the outside label of a product: