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Structure of 143679-80-5
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This chiral cyclopentane derivative features a protected amine and carboxylic acid group, enabling direct incorporation into peptide synthesis. The tert-butoxycarbonyl (Boc) moiety provides stability during reaction sequences, while the (1S,2S) stereochemistry ensures high diastereoselectivity in downstream coupling steps.
(1S,2S)-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid serves as a stereochemically defined building block for cyclopentane-based peptidomimetics and bioactive scaffolds. The Boc-protected amine enables straightforward functionalization and orthogonal deprotection, while the carboxylic acid supports coupling reactions with minimal epimerization. Its bench-stable, crystalline nature facilitates handling and purification in multi-step syntheses.
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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-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: