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Structure of 662139-46-0
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7-Bromoisoquinolin-3-ol features a brominated isoquinoline scaffold with a phenolic hydroxyl group, enabling direct functionalization in cross-coupling and cyclization reactions. The electron-deficient heterocycle facilitates metal-catalyzed transformations, while the hydroxyl moiety offers a handle for derivatization under mild conditions. This bench-stable compound serves as a key intermediate in medicinal chemistry and materials science.
7-Bromoisoquinolin-3-ol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C3 hydroxyl and C7 bromine positions. Its bench-stable structure supports palladium-catalyzed cross-coupling reactions and nucleophilic substitution protocols, facilitating efficient access to complex isoquinoline-based scaffolds relevant to kinase inhibitors and CNS-targeted therapeutics.
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Lot numbers can be found on the outside label of a product: