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Structure of 6484-24-8
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4-Chloro-2-methylquinazoline is a heterocyclic scaffold featuring a chlorine atom at the 4-position and a methyl group at the 2-position, enabling selective functionalization in medicinal chemistry. This electron-deficient core integrates readily into kinase inhibitor architectures and serves as a key building block for bioactive molecules in drug discovery pipelines.
4-Chloro-2-methylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its chloro group at the 4-position exhibits high reactivity in Suzuki, Stille, and Buchwald–Hartwig transformations, while the 2-methyl substituent enhances solubility and modulates electronic properties. The scaffold is bench-stable, easily purified by recrystallization, and functions as a core motif in kinase inhibitor development and heterocyclic library synthesis.
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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: