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Structure of 633328-95-7
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5-Bromo-2-chloro-4-methylpyrimidine serves as a key heterocyclic building block for medicinal chemistry and agrochemical synthesis. The molecule features orthogonal halogen substituents at C5 (bromine) and C2 (chlorine), enabling sequential cross-coupling reactions. The methyl group at C4 enhances electronic modulation and improves solubility in organic media. This compound exhibits bench-stable handling properties and integrates readily into complex molecular architectures under standard coupling conditions.
5-Bromo-2-chloro-4-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through palladium-catalyzed cross-coupling reactions. Its orthogonal halogen reactivity—bromine at C5 and chlorine at C2—facilitates sequential functionalization, while the methyl group at C4 enhances metabolic stability. The compound exhibits excellent bench stability, ease of purification, and broad compatibility with standard synthetic protocols, making it well-suited for both small-molecule discovery and process-scale applications.
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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: