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Structure of 20090-69-1
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2-Chloro-4-methylpyrimidin-5-amine delivers a reactive chloro handle and an electron-rich amine site within a stable pyrimidine scaffold. This bifunctional heterocycle integrates efficiently into medicinal chemistry campaigns, enabling rapid diversification through nucleophilic substitution or coupling reactions under standard conditions.
2-Chloro-4-methylpyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the amino and methyl functionalities offer orthogonal handles for further functionalization. The compound exhibits good bench stability and is compatible with standard coupling protocols, 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: