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Structure of 120737-78-2
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1-Boc-2-Methylpiperazine delivers a protected piperazine scaffold with enhanced stability and solubility in organic media. The tert-butoxycarbonyl group enables straightforward deprotection under mild acidic conditions, facilitating integration into complex molecular architectures. This bench-stable derivative simplifies handling during synthetic workflows involving nitrogen heterocycles.
1-Boc-2-methylpiperazine serves as a versatile nitrogen source in medicinal chemistry, enabling efficient construction of piperazine-based scaffolds. The Boc group provides excellent stability and ease of removal under mild acidic conditions, while the methyl substitution enhances solubility and modulates basicity. It functions reliably in amide coupling, reductive amination, and nucleophilic displacement reactions, offering predictable reactivity and straightforward purification—ideal for iterative synthesis and lead optimization workflows.
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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 : 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: