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Structure of 22864-65-9
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4-(Trifluoromethyl)-N-methylaniline features a trifluoromethyl group that imparts strong electron-withdrawing character, enhancing reactivity in electrophilic substitution. The N-methyl substitution improves solubility and metabolic stability, making this compound valuable for pharmaceutical intermediates and agrochemical synthesis.
4-(Trifluoromethyl)-N-methylaniline serves as a valuable building block in medicinal chemistry, enabling the introduction of both electron-withdrawing trifluoromethyl and amine functionalities in a single scaffold. Its stability under standard reaction conditions facilitates diverse transformations, including electrophilic substitution and coupling reactions, while the N-methyl group enhances metabolic stability and membrane permeability—key attributes for bioactive compound 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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: