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Structure of 937236-73-2
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Ethyl 2-(2-chloropyridin-4-yl)acetate features a pyridine ring bearing a chloro substituent at the 2-position and an acetyl ester group at the 4-position, enabling direct functionalization in cross-coupling reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring electron-deficient heterocyclic building blocks for pharmaceutical intermediates.
Ethyl 2-(2-chloropyridin-4-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-containing scaffolds. The electrophilic chloro group facilitates nucleophilic substitution reactions, while the ester functionality supports subsequent transformations such as hydrolysis, reduction, or coupling. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for iterative synthesis workflows in API 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-P405-P501
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Lot numbers can be found on the outside label of a product: