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Structure of 1216129-71-3
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Methyl 2-(2-chloropyrimidin-4-yl)acetate features a pyrimidine core functionalized with a chloro group at C2 and an acetyl ester side chain, enabling direct integration into pharmaceutical intermediates. The electron-deficient pyrimidine ring enhances reactivity in nucleophilic substitution cascades, while the methyl ester serves as a stable handle for subsequent transformations under standard conditions.
Methyl 2-(2-chloropyrimidin-4-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. The chloropyrimidine moiety facilitates nucleophilic substitution reactions, while the ester group supports subsequent transformations including hydrolysis, reduction, or coupling protocols. This compound exhibits good bench stability and is compatible with standard reaction conditions, making it well-suited for modular synthesis of bioactive heterocycles and API 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: