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Structure of 1598222-27-5
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4,6-Dibromo-2-methylpyrimidine features a highly reactive pyrimidine core with bromine substituents at the 4 and 6 positions, enabling efficient cross-coupling transformations. The methyl group at C2 enhances regioselectivity in nucleophilic substitutions. This bench-stable, moisture-tolerant building block facilitates rapid access to functionalized heterocycles in medicinal chemistry and materials science applications.
4,6-Dibromo-2-methylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted pyrimidine scaffolds. Its dual bromine sites facilitate Suzuki-Miyaura and Stille couplings under standard conditions, while the methyl group provides a handle for selective functionalization. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for iterative synthetic 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: