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Structure of 193902-87-3
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tert-Butyl 4-(4-amino-2-(trifluoromethyl)phenyl)piperazine-1-carboxylate features a trifluoromethyl-substituted aniline core paired with a piperazine scaffold, enabling efficient integration into bioactive molecules. The tert-butyl ester group offers stability and convenient deprotection under mild acidic conditions, streamlining synthetic workflows in medicinal chemistry.
tert-Butyl 4-(4-amino-2-(trifluoromethyl)phenyl)piperazine-1-carboxylate serves as a key intermediate in the synthesis of bioactive heterocycles, enabling efficient construction of trifluoromethylated phenylpiperazine scaffolds. Its tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The molecule exhibits robust functional group tolerance, supporting diverse coupling reactions and further derivatization in medicinal chemistry campaigns.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: