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Structure of 6323-18-8
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This 1-(2-chlorophenyl)propan-1-one features a chlorinated aromatic ring paired with a ketone-functionalized alkyl chain, enabling direct incorporation into synthetic pathways requiring electron-deficient aryl groups. The molecule exhibits robust stability under standard bench conditions and facilitates efficient coupling reactions in pharmaceutical intermediates and functional materials.
1-(2-Chlorophenyl)propan-1-one serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient construction of biologically relevant scaffolds. Its aryl ketone functionality supports electrophilic functionalization, Grignard additions, and reductive transformations under standard conditions. The ortho-chloro substituent enhances metabolic stability and provides a handle for further derivatization via cross-coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in multistep syntheses and process development workflows.
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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: