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Structure of 14394-60-6
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2-Chloro-6-methylpyrimidin-4-ylamine features a pyrimidine core bearing a chlorine at C2, a methyl group at C6, and an amino substituent at C4, enabling direct integration into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in medicinal chemistry, particularly for kinase inhibitors and antiviral agents, where its electron-deficient ring facilitates nucleophilic substitution reactions under mild conditions.
2-Chloro-6-methylpyrimidin-4-ylamine 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 primary amine supports direct coupling or derivatization. The molecule exhibits good bench stability and functional group tolerance, making it well-suited for iterative synthesis workflows and scale-up applications in API development.
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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: