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Structure of 354574-56-4
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4-Bromo-2,6-dimethylpyrimidine serves as a key building block in medicinal chemistry, featuring a sterically hindered pyrimidine core with bromine at the C4 position and methyl groups flanking the ring. This combination enables selective cross-coupling reactions and facilitates the synthesis of bioactive heterocycles under standard conditions.
4-Bromo-2,6-dimethylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyrimidines via palladium-catalyzed cross-coupling reactions. Its bromine substituent facilitates reliable C–C bond formation under standard Suzuki or Stille conditions, while the methyl groups enhance metabolic stability and modulate electronic properties. The compound exhibits excellent bench stability, simplifies purification, and functions effectively in multi-step syntheses of kinase inhibitors and other bioactive 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-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: