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Structure of 394735-65-0
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This chiral building block features a bench-stable tert-butoxycarbonyl-protected amine paired with a sterically hindered 4,4-difluorocyclohexyl moiety. The electron-deficient cyclohexane ring enhances metabolic stability, while the carboxylic acid functionality enables efficient coupling reactions in peptide synthesis and medicinal chemistry applications.
(S)-2-((tert-Butoxycarbonyl)amino)-2-(4,4-difluorocyclohexyl)acetic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. The protected amino group enables orthogonal functionalization, while the 4,4-difluorocyclohexyl moiety imparts metabolic stability and modulates lipophilicity. Its bench-stable tert-butyl carbamate protection simplifies purification, and the molecule readily participates in standard coupling reactions, facilitating access to complex scaffolds with high stereocontrol.
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Lot numbers can be found on the outside label of a product: