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Structure of 66131-68-8
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2-Chloro-N-methylpyrimidin-4-amine features a reactive chlorine at the C2 position and a methylated nitrogen at the N1 site, enabling selective coupling in cross-coupling and nucleophilic substitution reactions. The electron-deficient pyrimidine ring enhances reactivity toward amines and thiols, while the N-methyl group improves solubility and stability under standard conditions.
2-Chloro-N-methylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions with amines, thiols, and other heteroatom nucleophiles, while the N-methylpyrimidin-4-amine core provides a stable, bench-stable platform for further functionalization. Its compatibility with standard coupling protocols and predictable reactivity profile make it ideal for modular synthesis of kinase inhibitors and other bioactive compounds.
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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-H319
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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: