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Structure of 98556-31-1
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4-Chloro-6-iodoquinazoline is a halogenated quinazoline derivative featuring complementary reactive sites at the 4-chloro and 6-iodo positions. This dual functionality enables selective cross-coupling transformations in synthetic routes to biologically active molecules. The compound exhibits stability under standard handling conditions and serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors.
4-Chloro-6-iodoquinazoline serves as a versatile bifunctional building block for transition-metal-catalyzed cross-coupling reactions. The chloro group enables palladium-catalyzed coupling with boronic acids, while the iodo substituent supports efficient Suzuki-Miyaura or Stille transformations under mild conditions. This complementary reactivity profile facilitates rapid diversification of quinazoline scaffolds in medicinal chemistry and agrochemical research. The compound exhibits good bench stability and is readily purified by flash chromatography, supporting its utility in multi-step syntheses.
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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: