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Structure of 27687-14-5
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trans-4-(((tert-Butoxycarbonyl)amino)methyl)cyclohexanecarboxylic acid features a sterically defined cyclohexane scaffold with a bench-stable Boc-protected amino-methyl side chain. This configuration enables direct incorporation into peptide synthesis workflows, where the protected amine facilitates sequential coupling without racemization. The rigid trans-configuration enhances conformational control in cyclic peptide architectures.
trans-4-(((tert-Butoxycarbonyl)amino)methyl)cyclohexanecarboxylic acid serves as a versatile, bench-stable building block for the synthesis of bioactive cyclohexyl-containing scaffolds. The protected amine and carboxylic acid functionalities enable sequential functionalization in peptide and heterocyclic chemistry, while the trans-cyclohexane conformation provides defined stereochemical control. Its stability under standard reaction conditions facilitates purification and integration into multi-step syntheses.
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Lot numbers can be found on the outside label of a product: