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Structure of 1097779-00-4
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Methyl 2-(6-chloropyrimidin-4-yl)acetate features a chloropyrimidine core linked to a methyl acetate group, enabling direct incorporation into heterocyclic scaffolds. This bench-stable, moisture-tolerant reagent facilitates efficient coupling reactions in medicinal chemistry workflows. The electron-deficient pyrimidine ring enhances reactivity toward nucleophiles, streamlining access to bioactive derivatives.
Methyl 2-(6-chloropyrimidin-4-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloropyrimidine moiety facilitates nucleophilic substitution reactions, while the ester group offers compatibility with standard functional group manipulations. Its bench-stable nature and straightforward purification make it well-suited for use in multi-step syntheses targeting kinase inhibitors and antiviral agents.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: