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Structure of 857280-53-6
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1-Phenylazetidin-3-ol features a strained azetidine ring fused to a phenyl group and a hydroxyl-bearing carbon, delivering high reactivity for conjugate additions. This scaffold integrates readily into bioactive molecules, offering enhanced metabolic stability and polarity compared to larger heterocycles. The hydroxyl moiety enables downstream functionalization through etherification or oxidation pathways.
1-Phenylazetidin-3-ol serves as a valuable chiral building block for the synthesis of β-lactam-containing pharmaceuticals and agrochemicals. Its azetidine core exhibits enhanced ring strain, enabling efficient functionalization at the C3 position. The hydroxyl group provides a handle for derivatization while maintaining good bench stability and compatibility with standard protecting group strategies. This compound functions effectively in nucleophilic transformations and facilitates the construction of complex heterocyclic scaffolds under mild conditions.
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Lot numbers can be found on the outside label of a product: