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Structure of 1749-68-4
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6-Chloro-2-methylpyrimidin-4-amine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorinated pyrimidine core with a methyl group at C2 and an amino function at C4. This combination enables efficient coupling in transition-metal-catalyzed reactions, facilitating the construction of advanced pharmaceutical intermediates under standard conditions.
6-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 C6 and amino group at C4 provide orthogonal reactivity for sequential functionalization, while the methyl substituent enhances metabolic stability. Bench-stable and readily purified, it facilitates scalable synthesis of kinase inhibitors and other bioactive heterocycles.
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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: