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Structure of 22246-12-4
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6-Methoxy-3,4-dihydroisoquinolin-1(2H)-one features a fused heterocyclic core with a methoxy group at the 6-position, enhancing solubility and electronic modulation. This scaffold integrates readily into bioactive molecule design, offering stability under standard conditions and compatibility with diverse synthetic transformations.
6-Methoxy-3,4-dihydroisoquinolin-1(2H)-one serves as a versatile scaffold in medicinal chemistry, enabling efficient access to bioactive isoquinoline derivatives. Its bench-stable structure features a protected carbonyl and methoxy substituent that tolerate diverse transformations, including hydrogenation, electrophilic substitution, and palladium-catalyzed coupling. The functional group pattern supports modular synthesis of heterocyclic libraries and provides orthogonal reactivity for downstream derivatization.
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Lot numbers can be found on the outside label of a product: