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Structure of 851986-00-0
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4,6-Dichloro-5-methoxy-2-methylpyrimidine features a highly reactive pyrimidine core with dual chlorines at C4 and C6, enabling efficient cross-coupling and nucleophilic substitution. The methoxy and methyl groups enhance solubility and stabilize the molecule under standard conditions. This compound serves as a key building block in agrochemical and pharmaceutical synthesis, particularly for heterocyclic systems requiring selective functionalization.
4,6-Dichloro-5-methoxy-2-methylpyrimidine serves as a versatile pyrimidine-based building block for medicinal chemistry and agrochemical synthesis. Its orthogonal reactivity enables selective functionalization at C4 and C6 positions, while the methoxy and methyl groups provide steric and electronic modulation. The compound exhibits excellent bench stability and facilitates efficient coupling reactions in standard protocols, making it well-suited for constructing complex heterocyclic scaffolds via nucleophilic substitution or transition-metal-catalyzed transformations.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301+H311+H331
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Precautionary Statements : P233-P261-P264-P270-P271-P280-P302+P352-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: