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Structure of 954220-98-5
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2,4-Dichloro-5-fluoro-6-methylpyrimidine features a highly functionalized pyrimidine core with orthogonal halogen and methyl substituents enabling selective cross-coupling and derivatization. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, particularly for kinase inhibitors and nucleoside analogs. The strategic placement of chlorine and fluorine atoms enhances reactivity while maintaining stability under standard conditions.
2,4-Dichloro-5-fluoro-6-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic substitution and cross-coupling reactions. The strategically positioned chlorine and fluorine atoms facilitate selective functionalization, while the methyl group enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for scalable synthesis of kinase inhibitors and other bioactive molecules.
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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: