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Structure of 4590-52-7
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7-Fluoro-3,4-dihydroquinolin-2(1H)-one features a fluorinated quinolinone core with enhanced electron-withdrawing character due to the para-fluorine substitution. This scaffold integrates readily into medicinal chemistry libraries, offering improved metabolic stability and membrane permeability. The saturated ring system provides conformational rigidity beneficial for target binding.
7-Fluoro-3,4-dihydroquinolin-2(1H)-one serves as a versatile heterocyclic scaffold in medicinal chemistry, enabling efficient access to bioactive molecules through established functionalization at the 2-position and C3–C4 ring system. Its fluorinated aromatic core enhances metabolic stability and modulates electronic properties, while the lactam functionality supports diverse transformations including nucleophilic substitution and transition-metal-catalyzed coupling. Bench-stable and amenable to purification via standard chromatography, it functions as a reliable building block for targeted synthesis of pharmaceutical intermediates and CNS-active compounds.
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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: