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Structure of 479353-63-4
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1-Boc-4-(4-carboxybenzyl)piperazine features a protected piperazine core linked to a para-carboxybenzyl moiety, enabling direct conjugation in peptide and macrocyclic synthesis. The Boc group ensures stability during reaction sequences, while the carboxylic acid facilitates amide coupling or derivatization under standard conditions.
1-Boc-4-(4-carboxybenzyl)piperazine serves as a versatile building block for medicinal chemistry and peptide conjugation, enabling direct incorporation of a carboxylic acid-functionalized piperazine motif. The Boc group provides excellent bench stability and orthogonal protection, facilitating selective deprotection under mild acidic conditions. It readily participates in amide coupling reactions and functions as a key scaffold in the synthesis of bioactive molecules, including kinase inhibitors and GPCR modulators, with high functional group tolerance and ease of purification.
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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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: