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Structure of 1636-34-6
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This diphenylbutane diol features two adjacent hydroxyl groups flanked by aryl-substituted carbon centers, delivering enhanced stability and solubility in organic media. The rigid, sterically congested backbone facilitates selective transformations in asymmetric synthesis and serves as a chiral scaffold for ligand development.
2,3-Diphenylbutane-2,3-diol serves as a valuable chiral synthon in asymmetric synthesis, enabling stereoselective transformations through its rigid, geminally disubstituted diol framework. Its bench-stable nature and tolerance to common functional groups facilitate straightforward purification and integration into multi-step sequences. The molecule functions effectively in oxidation, protection, and coupling reactions, particularly in the construction of complex heterocyclic scaffolds and biaryl architectures relevant to medicinal chemistry.
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Lot numbers can be found on the outside label of a product: