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Structure of 300374-83-8
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This trifluoromethyl ketone features a 3,4-dimethoxyphenyl group that enhances solubility and electron density, enabling efficient coupling in C–C bond formation. The electron-deficient trifluoromethyl moiety facilitates nucleophilic addition, while the bench-stable structure supports reliable handling under standard conditions.
1-(3,4-Dimethoxyphenyl)-2,2,2-trifluoroethanone serves as a versatile building block in medicinal chemistry, enabling efficient access to trifluoromethylated aryl ketones via standard carbonyl transformations. Its stability under ambient conditions and compatibility with common coupling reactions facilitate straightforward incorporation into complex molecular architectures. The molecule functions effectively in nucleophilic addition and conjugate addition protocols, offering reliable access to functionalized heterocycles and bioactive scaffolds.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: