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Structure of 1802790-53-9
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This piperidine derivative features a tert-butoxycarbonyl-protected amine and a cyanomethyl group positioned at the 4-position, enabling direct incorporation into peptide synthesis. The electron-withdrawing nitrile enhances reactivity in coupling reactions while maintaining stability under standard bench conditions.
1-(tert-Butoxycarbonyl)-4-(cyanomethyl)piperidine-4-carboxylic acid serves as a versatile building block for the synthesis of piperidine-based scaffolds in medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides excellent stability and orthogonal deprotection, while the cyanomethyl functionality enables subsequent transformations such as hydrolysis, reduction, or cyclization. This compound facilitates efficient access to functionalized piperidines under standard peptide coupling and reductive amination conditions, offering reliable performance in both small-molecule and API development workflows.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: