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Structure of 724422-42-8
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6-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one features a brominated isoquinoline core with a methyl substituent at the 2-position, enabling direct functionalization in late-stage synthesis. The lactam moiety enhances solubility and stability under standard conditions, while the electron-deficient aromatic system facilitates transition-metal-catalyzed coupling reactions. This scaffold serves as a key intermediate in medicinal chemistry campaigns targeting CNS modulators and kinase inhibitors.
6-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one serves as a versatile scaffold for medicinal chemistry and synthetic organic applications. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the lactam functionality offers hydrogen-bonding capacity and structural rigidity. Bench-stable and compatible with diverse functional groups, it facilitates efficient access to complex heterocyclic architectures through modular transformations.
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Lot numbers can be found on the outside label of a product: