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Structure of 2338-56-9
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4-Fluoro-2,6-dimethylphenol features a fluorine atom at the para position relative to a hydroxyl group, flanked by two methyl substituents that enhance electron density and steric protection. This configuration imparts improved stability and solubility in organic solvents, enabling efficient incorporation into pharmaceutical intermediates and functional materials under standard conditions.
4-Fluoro-2,6-dimethylphenol serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering a sterically hindered aryl scaffold with orthogonal functional handles. The fluorine substituent enhances metabolic stability and modulates electronic properties, while the phenolic hydroxyl enables direct derivatization via etherification or esterification. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to complex heterocyclic systems and API intermediates.
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Lot numbers can be found on the outside label of a product: