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Structure of 107070-69-9
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1-[4-(Dimethylamino)-2-hydroxyphenyl]ethan-1-one features a conjugated enone system flanked by a strongly electron-donating dimethylamino group and a phenolic hydroxyl, enhancing its reactivity in nucleophilic addition processes. The compound exhibits enhanced solubility in polar organic solvents and stability under standard bench conditions, enabling straightforward integration into synthetic workflows for advanced intermediates.
1-[4-(Dimethylamino)-2-hydroxyphenyl]ethan-1-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and functionalized aryl ketones. Its ortho-hydroxyl and para-dimethylamino groups facilitate metal-catalyzed coupling reactions and intramolecular cyclizations, while the ketone functionality supports nucleophilic additions and enolization under mild conditions. The compound exhibits good bench stability and is amenable to standard purification techniques, making it suitable for iterative synthetic workflows in API development.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
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Lot numbers can be found on the outside label of a product: