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Structure of 201810-59-5
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This protected bipiperidine derivative features a tert-butoxycarbonyl group that enables stable incorporation into peptide and small-molecule syntheses. The carboxylic acid functionality provides a reactive handle for amide coupling, while the rigid piperidine scaffold offers defined conformational control in bioactive compound design.
1'-(tert-Butoxycarbonyl)-[1,4'-bipiperidine]-4-carboxylic acid serves as a versatile building block for the synthesis of complex nitrogen-containing scaffolds. The Boc-protected piperidine moiety enables stable storage and orthogonal deprotection, while the carboxylic acid functionality facilitates amide coupling and conjugation reactions. This compound functions effectively in solid-phase synthesis and solution-phase diversification, offering excellent 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-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: