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Structure of 393-11-3
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for synthesis
4-Nitro-3-(trifluoromethyl)aniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to functionalized aromatic scaffolds. Its electron-deficient aryl core facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions. The nitro group offers direct reduction to an amine for further derivatization, while the trifluoromethyl moiety enhances metabolic stability and lipophilicity. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows.
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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: