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Structure of 351426-04-5
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6-Bromo-4-chloro-2-methylquinazoline features a sterically accessible quinazoline core with complementary halogenation and methyl substitution. This configuration enables direct functionalization in cross-coupling reactions, delivering diverse heterocyclic architectures under standard conditions. The electron-deficient ring system enhances reactivity in Pd-catalyzed transformations while maintaining bench-stable handling properties.
6-Bromo-4-chloro-2-methylquinazoline serves as a versatile building block for the synthesis of kinase inhibitors and other bioactive heterocycles. Its complementary halogenation pattern enables palladium-catalyzed cross-coupling reactions with high efficiency, while the methyl group provides a site for further functionalization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for both medicinal chemistry and process-scale applications.
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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: