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Structure of 6627-22-1
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Methyl 6-chloropyrimidine-4-carboxylate features a chlorinated pyrimidine core with a methyl ester at C4, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in medicinal chemistry, particularly for constructing kinase inhibitors and antiviral agents through cross-coupling or nucleophilic substitution reactions.
Methyl 6-chloropyrimidine-4-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group at C6 facilitates nucleophilic substitution reactions, while the ester functionality supports selective transformations and derivatization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for multi-step synthesis workflows targeting heterocyclic APIs and functionalized intermediates.
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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: