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Structure of 1259224-17-3
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3-Bromoquinoline-7-carbaldehyde features a quinoline core with strategically positioned bromo and formyl groups, enabling direct functionalization in cross-coupling and heterocycle synthesis. The electron-deficient aldehyde facilitates nucleophilic additions, while the bromine serves as a reactive handle for palladium-catalyzed transformations. This scaffold combines high reactivity with bench-stable handling properties, making it ideal for building complex molecular architectures in medicinal chemistry and materials science.
3-Bromoquinoline-7-carbaldehyde serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling direct functionalization at the quinoline core. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the aldehyde functions as a key handle for reductive amination, imine formation, or oxime derivatization. Its bench-stable nature and compatibility with diverse reaction conditions support efficient access to complex heterocyclic scaffolds relevant to drug discovery.
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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: