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Structure of 19815-17-9
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4-Chloro-7-nitroquinazoline features a fused bicyclic core with complementary electron-withdrawing groups at the 4-chloro and 7-nitro positions, enabling selective reactivity in cross-coupling and bioconjugation workflows. This bench-stable scaffold integrates readily into kinase inhibitor libraries and serves as a key intermediate for targeted covalent probe development under standard conditions.
4-Chloro-7-nitroquinazoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions at the C4 position due to its activated halide. The electron-withdrawing nitro group at C7 enhances electrophilicity and facilitates nucleophilic substitution, while the quinazoline core provides a rigid scaffold for targeted drug discovery. Its bench-stable nature and compatibility with standard reaction conditions make it suitable for iterative synthesis of kinase inhibitors and other heterocyclic APIs.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H318-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: