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Structure of 931-61-3
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N-Methylpyrimidin-2-amine features a pyrimidine core with a methylated nitrogen at the 2-position, delivering enhanced solubility and metabolic stability. This bench-stable heterocycle integrates readily into pharmaceutical scaffolds, serving as a key building block in kinase inhibitor development and medicinal chemistry campaigns.
N-Methylpyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its methylated nitrogen enhances solubility and metabolic stability while maintaining reactivity for palladium-catalyzed cross-coupling reactions. The compound functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive heterocycles, offering excellent bench stability and compatibility with standard purification methods.
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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: