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Structure of 22536-67-0
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2,5-Dichloropyrimidine serves as a pivotal building block in medicinal chemistry and materials synthesis. This electron-deficient heterocycle features two chlorine substituents at the 2- and 5-positions, enabling efficient nucleophilic substitution reactions. The molecule exhibits high reactivity under mild conditions and maintains bench-stability, facilitating its integration into diverse molecular architectures.
2,5-Dichloropyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization at C2 and C5 positions via nucleophilic substitution. Its high reactivity facilitates the construction of substituted pyrimidines under mild conditions, with excellent functional group tolerance and bench stability. Widely used in the synthesis of kinase inhibitors and heterocyclic APIs, it functions as a key intermediate in cross-coupling and amine displacement reactions.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: