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Structure of 178445-83-5
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This chalcone derivative features a conjugated enone system flanked by electron-rich aromatic rings, enhancing its stability and reactivity in synthetic transformations. The 3,4-dimethoxyphenyl moiety imparts solubility and resistance to oxidation, while the phenolic hydroxyl group enables further derivatization or metal coordination. Designed for use in natural product synthesis and medicinal chemistry screening.
3-(3,4-Dimethoxyphenyl)-1-(3-hydroxyphenyl)propan-1-one serves as a versatile scaffold for the synthesis of bioactive molecules, leveraging its conjugated enone system and multiple aromatic functional groups. The molecule enables efficient Michael additions, electrophilic substitutions, and transition-metal-catalyzed couplings due to its well-defined reactivity profile. Bench-stable and readily purified via crystallization, it functions as a key building block in natural product analogs and pharmaceutical intermediates requiring ortho-hydroxyl and methoxy-directed transformations.
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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 : P233-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: