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Structure of 67818-41-1
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1-(2-Chloro-4-nitrophenyl)ethanone features a chlorinated, electron-deficient aryl core paired with a reactive acetyl group, enabling direct integration into electrophilic coupling and C–C bond-forming reactions. This bench-stable ketone serves as a key intermediate in the synthesis of functionalized heterocycles and pharmaceutical scaffolds.
1-(2-Chloro-4-nitrophenyl)ethanone serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biologically relevant heterocycles and functionalized aromatic systems. Its dual electron-withdrawing groups (chloro and nitro) enhance electrophilicity at the aryl ring, facilitating nucleophilic substitution and coupling reactions. The ketone functionality provides a handle for further derivatization via enolization or reduction. Bench-stable and readily purified by recrystallization, it functions reliably in multistep syntheses targeting pharmaceutical intermediates and agrochemical scaffolds.
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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: