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Structure of 1268810-09-8
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tert-Butyl (1-ethynylcyclopropyl)carbamate features a strained cyclopropyl ring tethered to an ethynyl group, enabling efficient copper-catalyzed azide-alkyne cycloaddition. This stable, bench-ready building block integrates seamlessly into click chemistry workflows, delivering high-yielding triazole formation under mild conditions.
tert-Butyl (1-ethynylcyclopropyl)carbamate serves as a stable, bench-ready building block for the synthesis of cyclopropyl-substituted heterocycles and bioactive molecules. Its terminal alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid access to triazole-linked scaffolds. The carbamate group provides orthogonal protection for amines, allowing selective deprotection under mild conditions. This reagent exhibits excellent functional group tolerance and is compatible with diverse reaction environments, making it ideal for modular synthetic strategies in medicinal chemistry and process development.
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Lot numbers can be found on the outside label of a product: