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Structure of 74173-76-5
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2,4-Dichloro-6-iodoquinazoline features a halogenated quinazoline core with complementary reactivity at the 6-position. This electron-deficient scaffold enables direct coupling in palladium-catalyzed cross-coupling reactions, delivering functionalized quinazolines under mild conditions. The molecule exhibits bench-stable handling and compatibility with diverse reaction environments.
2,4-Dichloro-6-iodoquinazoline serves as a versatile building block for the synthesis of quinazoline-based pharmaceutical intermediates. The molecule enables palladium-catalyzed cross-coupling reactions due to its iodine functionality, while the dichloro substituents offer sites for selective nucleophilic substitution. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient access to diverse heterocyclic scaffolds in medicinal chemistry 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: