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Structure of 1092348-26-9
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5-Chloro-7-fluoro-3,4-dihydronaphthalen-1(2H)-one features a fused bicyclic core with complementary halogen substituents enabling selective functionalization. The electron-deficient dihydronaphthalene scaffold supports efficient coupling reactions and serves as a key intermediate in bioactive compound synthesis. This bench-stable ketone integrates readily into medicinal chemistry campaigns requiring halogenated aromatic motifs.
5-Chloro-7-fluoro-3,4-dihydronaphthalen-1(2H)-one serves as a versatile scaffold for the synthesis of bioactive molecules, leveraging its electron-deficient aromatic core and strategically positioned halogen substituents. The ketone functionality enables direct nucleophilic addition or enolate formation, while the chlorine and fluorine atoms support palladium-catalyzed cross-coupling reactions. This compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate development.
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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-H320-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: