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Structure of 76228-06-3
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6-Bromo-2,3-dihydroquinolin-4(1H)-one features a brominated dihydroquinolinone core with enhanced reactivity at the C6 position. This bench-stable heterocycle integrates readily into cross-coupling and cyclization workflows, offering efficient access to complex nitrogen-containing scaffolds in medicinal chemistry and materials synthesis.
6-Bromo-2,3-dihydroquinolin-4(1H)-one serves as a versatile building block for the synthesis of biologically relevant heterocycles and pharmaceutical intermediates. Its bromine substituent enables facile palladium-catalyzed cross-coupling reactions, while the enaminone functionality supports electrophilic substitution and condensation processes. The compound exhibits good bench stability and is readily purified by crystallization, facilitating its use in multi-step synthetic sequences targeting kinase inhibitors and CNS-active compounds.
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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: