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Structure of 947684-78-8
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(R)-1-Boc-2-benzyl-piperazine features a stereochemically defined piperazine core with a tert-butoxycarbonyl group at the N1 position and a benzyl substituent at N2. This configuration enhances metabolic stability and facilitates downstream functionalization in medicinal chemistry. The Boc protection enables selective deprotection under mild acidic conditions, streamlining synthesis of bioactive piperazine derivatives.
(R)-1-Boc-2-benzyl-piperazine serves as a stereochemically defined building block for the synthesis of bioactive piperazine derivatives. Its Boc group provides stability and ease of deprotection under mild acidic conditions, while the benzyl moiety offers orthogonal protection and enhanced solubility. The molecule facilitates efficient functionalization in medicinal chemistry workflows, enabling access to diverse heterocyclic scaffolds through standard coupling and cyclization reactions.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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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: