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Structure of 887592-02-1
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4-Chloro-6,7-difluoro-2-methylquinazoline features a highly electron-deficient quinazoline core with strategic halogen and methyl substitutions. This scaffold enables direct integration into medicinal chemistry campaigns, particularly for kinase inhibitor development. The difluoro substitution enhances metabolic stability while the chloro group provides a reactive handle for palladium-catalyzed coupling. Bench-stable and moisture-tolerant, it simplifies handling in diverse synthetic workflows.
4-Chloro-6,7-difluoro-2-methylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient access to kinase inhibitor scaffolds. Its electron-deficient quinazoline core facilitates nucleophilic substitution reactions, particularly at the C4-chloro position, and exhibits excellent bench stability. The 6,7-difluoro substitution enhances metabolic stability and modulates electronic properties, while the 2-methyl group provides steric control during downstream functionalization. This compound functions effectively in standard coupling protocols and is well-suited for parallel synthesis campaigns targeting biologically active heterocycles.
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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-H320-H335
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: