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Structure of 170911-92-9
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tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate features a piperazine core linked to a para-aminophenyl group, delivering a robust scaffold for medicinal chemistry. The tert-butyl ester moiety enhances solubility and stability while enabling straightforward deprotection under mild acidic conditions. This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly those targeting CNS disorders and kinase pathways.
tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate serves as a versatile building block for the synthesis of biologically active piperazine-based compounds. Its robust tert-butoxycarbonyl (Boc) group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The pendant aniline functionality enables direct coupling reactions, including Suzuki-Miyaura, Ullmann, and reductive amination, making it ideal for constructing diverse heterocyclic scaffolds and drug candidates in medicinal chemistry 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 : 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: