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Structure of 4295-36-7
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2,3-Dihydroquinolin-4(1H)-one features a fused bicyclic scaffold with a lactam carbonyl and saturated C2–C3 bond, offering enhanced stability and solubility in polar solvents. This core structure integrates readily into synthetic routes for bioactive molecules, particularly in medicinal chemistry campaigns targeting kinase inhibitors and CNS modulators. The system’s electron-rich aromatic ring supports efficient functionalization at C6 and C7 positions.
2,3-Dihydroquinolin-4(1H)-one serves as a versatile scaffold in medicinal chemistry, enabling efficient access to bioactive heterocycles through standard functionalization at the C2 and C3 positions. Its bench-stable nature and compatibility with common coupling reactions facilitate rapid diversification. Functions as a key building block for synthesizing substituted quinolines and analogs relevant to kinase inhibitors and CNS-targeted therapeutics.
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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: