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Structure of 438249-95-7
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5-Chloro-2-methylpyrimidin-4-amine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorinated pyrimidine core with a methyl group at the 2-position and a primary amine at C4. This configuration enables efficient coupling reactions and enhances metabolic stability in bioactive molecule design. The compound demonstrates excellent solubility under standard conditions and exhibits robust bench-stability, facilitating its use in multi-step synthetic sequences.
5-Chloro-2-methylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its chlorine at C5 and amino group at C4 provide orthogonal reactivity for sequential functionalization, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for high-throughput synthesis and API development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: