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Structure of 32998-03-1
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2,6-Dichloro-N-methylpyrimidin-4-amine features a pyrimidine core bearing two chlorine substituents at the 2 and 6 positions and a methylamino group at the 4 position. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, enabling efficient coupling reactions for the synthesis of kinase inhibitors and other bioactive molecules. The compound exhibits enhanced stability under standard bench conditions and facilitates straightforward functionalization via nucleophilic substitution.
2,6-Dichloro-N-methylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its dichloro substitution pattern facilitates directed metalation and cross-coupling reactions, while the N-methyl group enhances metabolic stability and modulates solubility. The compound exhibits excellent bench stability and compatibility with standard functional groups, making it well-suited for modular 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: