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Structure of 406204-90-8
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6-Bromo-2,4-dichloroquinoline features a highly electron-deficient quinoline core functionalized with bromo and dichloro substituents at strategic positions. This scaffold enables direct coupling in cross-coupling reactions, serving as a key building block for pharmaceutical intermediates and advanced materials. The molecule exhibits enhanced stability under standard conditions and facilitates efficient derivatization through palladium-catalyzed processes.
6-Bromo-2,4-dichloroquinoline serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromine at the 6-position facilitates selective functionalization while the 2,4-dichloro substitution pattern ensures compatibility with standard coupling protocols. Its bench-stable nature and ease of purification make it ideal for constructing complex heterocyclic scaffolds in API development and advanced organic 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: