MSE PRO rel-(3aR,4R,6aS)-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride, ≥97.0% Purity - MSE Supplies LLC

MSE PRO rel-(3aR,4R,6aS)-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride, ≥97.0% Purity

SKU: CM1371

  • $ 27995
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MSE PRO™ rel-(3aR,4R,6aS)-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride, ≥97.0% Purity

MSE PRO™ rel-(3aR,4R,6aS)-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride is a chiral pyrrolidine derivative with a well-defined stereochemistry, offering the (3aR,4R,6aS) enantiomer in high optical purity. The presence of the hydroxy group and the rigid cyclopentane ring system make this compound a versatile synthetic intermediate for the preparation of various nitrogen-containing heterocyclic compounds and pharmaceutically active molecules. As a chiral building block, it can be employed in enantioselective synthesis, enabling the construction of optically pure drugs, agrochemicals, and other biologically active compounds where stereochemical purity is crucial for potency and selectivity.

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Technical Specifications:

CAS No. 130657-47-5
Chemical name rel-(3aR,4R,6aS)-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride
  • (3aR,4R,6aS)-rel-octahydrocyclopenta[c]pyrrol-4-ol hydrochloride

  • (3aS,4S,6aR)-rel-Octahydrocyclopenta[c]pyrrol-4-ol hydrochloride
Molecular formula C7H14ClNO            
Pack size

250 mg (CM1371)

Molecular weight 163.65 g/mol
Purity ≥97.0% (NMR)
Appearance White to off-white solid
Storage  Store at room temperature


[1] Bhat, A. A., Singh, I., Tandon, N., & Tandon, R. (2023). Structure activity relationship (SAR) and anticancer activity of pyrrolidine derivatives: Recent developments and future prospects (A review). European Journal of Medicinal Chemistry246, 114954.

[2] Bellina, F., & Rossi, R. (2006). Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions. Tetrahedron62(31), 7213-7256.