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Structure of 956-02-5
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This chalcone derivative features a conjugated enone system linking electron-rich and electron-deficient aromatic rings, enabling facile Michael additions and Diels–Alder reactions. The para-chlorophenyl group enhances electrophilicity at the β-carbon, while the phenyl ring contributes π-stacking potential. Bench-stable under standard conditions, it integrates readily into synthetic sequences targeting heterocycles and bioactive scaffolds.
1-(4-Chlorophenyl)-3-phenyl-2-propen-1-one serves as a versatile chalcone scaffold for medicinal chemistry and materials science applications. Its conjugated enone system enables reliable Michael additions, Diels–Alder cycloadditions, and metal-catalyzed cross-coupling reactions. The molecule exhibits good bench stability, facilitates straightforward purification via recrystallization, and demonstrates broad functional group tolerance in standard synthetic 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: