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Structure of 23082-50-0
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1-(2-Chloro-5-nitrophenyl)ethanone features a chlorinated, electron-deficient aromatic ring paired with a reactive acetyl group. This structure enables direct incorporation into conjugate addition reactions and facilitates efficient coupling in heterocyclic synthesis under standard conditions.
1-(2-Chloro-5-nitrophenyl)ethanone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted heterocycles and pharmaceutical intermediates. Its reactivity profile—characterized by ortho-directing nitro and chloro groups—facilitates electrophilic substitution and palladium-catalyzed coupling reactions. The ketone functionality supports nucleophilic additions and reductions, offering a robust platform for diversification. Bench-stable and readily purified by recrystallization, it is well-suited for scalable synthesis and process 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-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: