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Structure of 1677-37-8
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6-Fluoro-4-hydroxyquinolin-2(1H)-one features a fluorinated quinolinone core with a strategically positioned hydroxyl group, enhancing its electronic profile for use in medicinal chemistry. The electron-withdrawing fluorine at the 6-position modulates reactivity and metabolic stability, while the enolic hydroxyl supports hydrogen bonding in target interactions. This scaffold serves as a key building block in developing kinase inhibitors and fluorescent probes.
6-Fluoro-4-hydroxyquinolin-2(1H)-one serves as a versatile scaffold in medicinal chemistry, enabling direct functionalization at the C4 position via nucleophilic substitution or transition-metal-catalyzed coupling. The fluorine substituent enhances metabolic stability and modulates electronic properties, while the hydroxyl group provides a handle for derivatization. This compound exhibits bench stability and compatibility with standard purification methods, facilitating integration into multi-step syntheses of kinase inhibitors and other bioactive heterocycles.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: