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Structure of 222530-39-4
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This cyclohexane-based amino acid derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling direct incorporation into peptide synthesis workflows. The stereochemistry at the 1R,3S positions ensures predictable conformational behavior in folded structures. Bench-stable and moisture-tolerant, it simplifies handling during solid-phase assembly.
(1R,3S)-3-((tert-Butoxycarbonyl)amino)cyclohexanecarboxylic acid serves as a stereochemically defined building block for cyclohexane-based peptidomimetics and bioactive scaffolds. The Boc-protected amine enables straightforward deprotection and coupling under standard peptide synthesis conditions, while the carboxylic acid facilitates amide bond formation. Its rigid, trans-fused cyclohexane framework offers predictable conformational control, enhancing utility in medicinal chemistry campaigns requiring defined spatial orientation of functional groups.
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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: