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Structure of 161601-29-2
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This chiral cyclopentane-based building block features a protected amine and carboxylic acid functional group, enabling straightforward incorporation into peptide-like scaffolds. The tert-butoxycarbonyl group provides stability during synthesis, while the (1S,3S) stereochemistry ensures precise spatial orientation for downstream applications in medicinal chemistry and macrocyclic compound development.
(1S,3S)-3-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid serves as a stereochemically defined building block for cyclopentane-based peptidomimetics and bioactive heterocycles. The Boc-protected amine enables facile deprotection under mild acidic conditions, while the carboxylic acid facilitates coupling reactions. Its rigid cyclopentane framework provides conformational constraint ideal for structure-activity studies, with excellent bench stability and compatibility in standard SPPS and solution-phase syntheses.
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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-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: