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Structure of 89466-39-7
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4-Chloro-6-methoxy-2-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorinated position at C4 and a methoxy group at C6. This electron-deficient pyrimidine core integrates readily into kinase inhibitors and antiviral agents. The methyl substitution at C2 enhances metabolic stability and modulates electronic properties. The compound exhibits excellent bench-stability and compatibility with standard coupling reactions under mild conditions.
4-Chloro-6-methoxy-2-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and cross-coupling reactions. The chloro group at C4 provides a reliable handle for functionalization, while the methoxy and methyl substituents enhance solubility and modulate electronic properties. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for multi-step synthesis and process development workflows.
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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: