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Structure of 7752-78-5
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5-Bromo-2-methylpyrimidine serves as a key heterocyclic scaffold for medicinal chemistry and agrochemical synthesis. The bromine at the 5-position enables efficient cross-coupling reactions, while the methyl group enhances solubility and modulates electronic properties. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.
5-Bromo-2-methylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine substituent. The methyl group at the 2-position enhances electronic stability and facilitates selective functionalization. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing pharmaceutically relevant pyrimidine scaffolds and advanced intermediates in medicinal chemistry workflows.
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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: