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Structure of 579-74-8
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1-(2-Methoxyphenyl)ethanone features a benzene ring bearing both methoxy and acetyl substituents in ortho configuration, delivering enhanced solubility and stability under standard bench conditions. This electron-rich aryl ketone integrates readily into synthetic sequences involving nucleophilic addition or coupling reactions, offering predictable reactivity for medicinal chemistry and materials synthesis applications.
1-(2-Methoxyphenyl)ethanone serves as a versatile aryl ketone building block in medicinal chemistry and natural product synthesis. Its ortho-methoxy substitution enhances electrophilic reactivity while maintaining bench stability. The molecule facilitates efficient Friedel-Crafts acylations, nucleophilic additions, and transition-metal-catalyzed couplings, enabling rapid access to substituted benzene derivatives and heterocyclic scaffolds under standard reaction conditions.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: