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Structure of 1432514-84-5
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Tert-butyl 8-bromo-4-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate features a brominated, hydroxylated dihydroisoquinoline core with a bench-stable tert-butyl ester handle. This versatile scaffold integrates readily into transition-metal-catalyzed couplings and enables direct functionalization at the C8 position. The electron-deficient aromatic system supports selective derivatization in complex synthesis workflows.
Tert-butyl 8-bromo-4-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate serves as a versatile building block for the synthesis of substituted isoquinoline scaffolds. The molecule combines a bench-stable tert-butyl ester, a bromo handle for cross-coupling reactions, and a phenolic hydroxyl group enabling further derivatization. Its functional group tolerance facilitates sequential transformations in medicinal chemistry workflows, making it well-suited for constructing complex heterocyclic systems under standard reaction conditions.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: