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Structure of 7627-44-3
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2,4-Dichloro-5-(iodomethyl)pyrimidine features a reactive iodomethyl group flanked by electron-withdrawing chlorines, enabling efficient functionalization in nucleophilic substitution reactions. This bench-stable pyrimidine derivative integrates readily into synthetic sequences requiring selective C–C or C–heteroatom bond formation under mild conditions.
2,4-Dichloro-5-(iodomethyl)pyrimidine serves as a versatile bifunctional building block for C–H functionalization and cross-coupling strategies. The iodoalkyl side chain enables palladium-catalyzed coupling reactions, while the pyrimidine core provides orthogonal reactivity for further derivatization. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for modular synthesis of heterocyclic scaffolds in medicinal chemistry and agrochemical development.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P264-P271-P280-P301+P330+P331-P304+P340-P363-P501
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Lot numbers can be found on the outside label of a product: