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Structure of 22614-72-8
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7-Chloroquinolin-2(1H)-one features a chlorine-substituted quinoline core with a lactam functionality, delivering enhanced electron-withdrawing character and improved solubility in polar solvents. This scaffold serves as a key building block for medicinal chemistry campaigns targeting kinase inhibitors and antiparasitic agents, offering robust stability under standard bench conditions.
7-Chloroquinolin-2(1H)-one serves as a versatile scaffold for medicinal chemistry and materials science, enabling efficient derivatization at the C-3 position via nucleophilic substitution or transition-metal-catalyzed coupling. Its inherent stability, solubility in common organic solvents, and compatibility with diverse functional groups make it well-suited for high-throughput synthesis of quinolinone-based libraries. The chlorine substituent enhances electrophilicity for further functionalization, while the lactam moiety provides a rigid, planar framework ideal for target-directed design.
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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: