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Structure of 40439-76-7
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5-Chloro-4-methylpyrimidin-2-amine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorinated pyrimidine core with a methyl group at C4 and an amino function at C2. This combination delivers enhanced metabolic stability and favorable electronic properties, enabling efficient coupling in cross-coupling reactions and facilitating the synthesis of kinase inhibitors and antiviral agents.
5-Chloro-4-methylpyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its ortho-chloro and amino groups facilitate palladium-catalyzed cross-coupling reactions and nucleophilic substitution, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable synthesis and API development workflows.
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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#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: