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Structure of 56745-01-8
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5-Bromo-2,4-dichloro-6-methylpyrimidine serves as a key heterocyclic scaffold for medicinal chemistry and agrochemical synthesis. The molecule features a sterically accessible pyrimidine core with strategically positioned halogens and a methyl group, enabling selective cross-coupling reactions under standard conditions. This combination facilitates efficient derivatization in late-stage functionalization workflows.
5-Bromo-2,4-dichloro-6-methylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its orthogonal reactivity profile—bromine at C5 for coupling, chlorines at C2/C4 for selective displacement, and methyl group at C6 for derivatization—facilitates modular construction of pharmaceutical scaffolds. Bench-stable and readily purified by recrystallization, it supports scalable synthesis workflows in medicinal chemistry and process development.
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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: