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Structure of 1430938-32-1
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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 1- and 3-positions ensures high diastereoselectivity in coupling reactions, while the bulky tert-butyl group provides steric shielding and enhanced stability during handling.
(1R,3R)-3-{[(tert-Butoxy)carbonyl]amino}cyclohexane-1-carboxylic acid serves as a stereochemically defined building block for cyclohexane-based peptidomimetics and bioactive scaffolds. The Boc-protected amine and carboxylic acid functionalities enable sequential coupling and orthogonal deprotection, facilitating efficient synthesis of complex targets. Its bench-stable nature and compatibility with standard peptide coupling protocols make it well-suited for medicinal chemistry campaigns requiring conformationally constrained intermediates.
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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: