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Structure of 917025-00-4
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Ethyl 2-(2-chloropyrimidin-5-yl)acetate features a chlorinated pyrimidine core linked to an ethyl acrylate moiety, enabling direct incorporation into heterocyclic scaffolds. This electrophilic building block facilitates C–C bond formation under mild conditions, offering high reactivity in cross-coupling and nucleophilic substitution processes. The molecule exhibits excellent stability and solubility in common organic solvents, simplifying handling during synthetic workflows.
Ethyl 2-(2-chloropyrimidin-5-yl)acetate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and coupling reactions. The electrophilic chloro group at the 2-position facilitates robust functionalization under mild conditions, while the ester moiety supports further derivatization. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: