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Structure of 155899-66-4
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This tetrahydrocyclopenta[d][1,3]dioxol derivative features a stereodefined amino-alcohol motif with a rigid, fused bicyclic core. The 6-amino and 4-hydroxyl groups are positioned on adjacent ring systems, enabling directional functionalization. Bench-stable and moisture-tolerant, this scaffold integrates readily into chiral building blocks for medicinal chemistry and natural product synthesis.
(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-ol serves as a stereochemically defined, bench-stable building block for the synthesis of complex heterocyclic scaffolds. Its amino and hydroxyl functionalities enable diverse functionalization, including amide coupling and derivatization under mild conditions. The rigid cyclopentadiol core provides structural preorganization, facilitating its use in medicinal chemistry campaigns targeting bioactive molecules with constrained geometries.
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Lot numbers can be found on the outside label of a product: