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Structure of 13602-82-9
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N-(2-Chloropyridin-4-yl)acetamide features a chloropyridine core paired with an acetamide handle, enabling direct integration into transition metal-catalyzed cross-coupling reactions. This bench-stable scaffold delivers efficient access to functionalized pyridine derivatives under standard conditions.
N-(2-Chloropyridin-4-yl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based heterocycles. Its ortho-chloro group facilitates palladium-catalyzed cross-coupling reactions, while the acetamide functionality offers moderate stability and compatibility with diverse reaction conditions. The molecule functions effectively in late-stage functionalization and scaffold diversification workflows.
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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: