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Structure of 32084-59-6
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6-Bromo-4-hydroxyquinazoline features a bromine atom at the 6-position and a hydroxyl group at the 4-position, enabling direct functionalization in C–H activation and cross-coupling reactions. This electron-deficient scaffold integrates readily into kinase inhibitor frameworks and serves as a key intermediate in medicinal chemistry campaigns targeting purine analogs.
6-Bromo-4-hydroxyquinazoline serves as a versatile building block for the synthesis of bioactive quinazoline derivatives. The bromo group enables palladium-catalyzed cross-coupling reactions, while the hydroxyl functionality provides a site for derivatization or protection. This compound exhibits good bench stability and facilitates efficient access to kinase inhibitor scaffolds through standard coupling and cyclization protocols.
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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: