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Structure of 35999-20-3
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This electrophilic ketone features a para-methoxyphenyl group that enhances solubility and modulates reactivity. The chlorine substituent at the alpha position enables facile nucleophilic substitution, streamlining access to functionalized aromatic scaffolds in synthetic workflows.
3-Chloro-1-(4-methoxyphenyl)propan-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenylalkyl scaffolds. Its electrophilic carbonyl and activated α-halo position facilitate nucleophilic addition, condensation reactions, and C–C bond formation under mild conditions. The molecule exhibits good bench stability and compatibility with common protecting groups, simplifying purification and integration into multi-step syntheses of pharmaceutical intermediates and functionalized heterocycles.
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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: