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Structure of 1780-31-0
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2,4-Dichloro-5-methylpyrimidine serves as a key heterocyclic building block for medicinal chemistry and agrochemical synthesis. The molecule features two chlorine substituents at electron-deficient positions, enabling efficient cross-coupling reactions. Its methyl group enhances lipophilicity and metabolic stability, while the pyrimidine core provides a rigid scaffold for targeted molecular design. This compound exhibits excellent bench stability and compatibility with diverse reaction conditions.
2,4-Dichloro-5-methylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via nucleophilic substitution. The dichloro functionality provides orthogonal reactivity at C2 and C4 positions, facilitating sequential functionalization with amines, thiols, and other nucleophiles. Its methyl group enhances metabolic stability and modulates electronic properties, while the compound exhibits excellent bench stability and ease of purification—key advantages for scalable synthesis and process development.
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GHS Pictogram :
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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 : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: