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Structure of 811450-17-6
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Methyl 4-chloropyrimidine-2-carboxylate features a chlorinated pyrimidine core with a methyl ester at the C2 position, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient pyrimidine ring facilitates nucleophilic substitution reactions, while the ester group offers versatility in downstream transformations. This compound serves as a key intermediate in medicinal chemistry for synthesizing kinase inhibitors and antiviral agents.
Methyl 4-chloropyrimidine-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. The chloro group at the 4-position facilitates nucleophilic substitution reactions, while the ester functionality supports selective transformations. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for medicinal chemistry campaigns 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: