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Structure of 72531-23-8
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1-(4-Amino-2-chlorophenyl)ethanone features a chlorinated aromatic core paired with a pendant acetamido group, enabling integration into bioactive scaffolds. The para-amino functionality supports derivatization and conjugation, while the electron-withdrawing chlorine enhances reactivity in electrophilic substitution processes. This compound exhibits robust stability under standard bench conditions and facilitates efficient incorporation into pharmaceutical intermediates and functional materials.
1-(4-Amino-2-chlorophenyl)ethanone serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical scaffolds. Its amine and chloro functionalities enable diverse coupling reactions and electrophilic substitutions, while the acetophenone moiety supports facile functionalization via enolization or reduction. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring orthogonal reactivity.
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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: