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Structure of 871791-79-6
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3-Isopropoxy-azetidine features a strained four-membered azetidine ring bearing a pendant isopropoxy group, delivering enhanced nucleophilicity and solubility in polar organic media. This bench-stable heterocycle integrates readily into synthetic routes requiring constrained nitrogen scaffolds with tailored lipophilicity, enabling efficient incorporation into bioactive molecule frameworks under standard conditions.
3-Isopropoxyazetidine serves as a valuable building block in medicinal chemistry, enabling the construction of bioactive heterocycles through reliable ring-opening and coupling reactions. Its strained azetidine core enhances reactivity in nucleophilic substitutions, while the isopropoxy group provides steric bulk and modulates solubility. The compound exhibits good bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.
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Lot numbers can be found on the outside label of a product: