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Structure of 1109230-25-2
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5-Bromo-3,4-dihydroisoquinolin-1(2H)-one features a brominated isoquinolinone core with enhanced electron deficiency at the aromatic ring, enabling efficient coupling in transition-metal-catalyzed reactions. The lactam functionality provides polarity and structural rigidity, facilitating incorporation into bioactive scaffolds. This compound exhibits bench-stable handling properties and compatibility with common organic solvents.
5-Bromo-3,4-dihydroisoquinolin-1(2H)-one serves as a versatile building block for medicinal chemistry and heterocyclic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the lactam functionality provides stability and directional reactivity. This scaffold facilitates the construction of complex alkaloid frameworks and drug-like molecules, offering good bench stability, straightforward purification, and compatibility with common functional groups in iterative synthesis workflows.
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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: