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Structure of 287714-35-6
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Methyl 2-chloropyrimidine-5-carboxylate features a pyrimidine core bearing a chloro substituent at C2 and an ester group at C5, enabling selective functionalization in heterocyclic synthesis. This bench-stable reagent integrates readily into cross-coupling and nucleophilic substitution reactions, delivering valuable intermediates for agrochemical and pharmaceutical development.
Methyl 2-chloropyrimidine-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. The chloro group at C2 facilitates nucleophilic substitution, while the ester functionality supports selective transformations and derivatization. Its bench stability and compatibility with standard coupling reactions make it well-suited for medicinal chemistry campaigns and API intermediate 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: