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Structure of 951173-22-1
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cis-2-((tert-Butoxycarbonyl)amino)cyclobutanecarboxylic acid features a rigid, sterically constrained cyclobutane scaffold with a bench-stable Boc-protected amine. This configuration enables direct incorporation into peptidomimetic architectures, where the cis stereochemistry enforces defined backbone geometry and enhances metabolic stability in bioactive molecule design.
cis-2-((tert-Butoxycarbonyl)amino)cyclobutanecarboxylic acid serves as a valuable chiral building block for the synthesis of bioactive cyclobutane-containing scaffolds. The protected amine and carboxylic acid functionalities enable orthogonal derivatization, while the cis-configured cyclobutane ring provides conformational rigidity. Its bench-stable nature and compatibility with standard coupling and deprotection protocols facilitate efficient access to peptide-like structures and heterocyclic systems in medicinal chemistry workflows.
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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: