Cas no 1212822-72-4 (1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol)

1,2,3,3a,4,5,6,6a-Octahydrocyclopenta[c]pyrrol-4-ol is a bicyclic heterocyclic compound featuring a fused cyclopentane-pyrrolidine structure with a hydroxyl group at the 4-position. This scaffold is of significant interest in synthetic and medicinal chemistry due to its rigid, three-dimensional framework, which enhances binding affinity and selectivity in drug design. The presence of both nitrogen and oxygen functionalities allows for versatile derivatization, making it a valuable intermediate for the development of bioactive molecules, particularly in central nervous system (CNS) and antiviral research. Its stereochemistry and conformational stability further contribute to its utility in asymmetric synthesis and chiral ligand design.
1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol structure
1212822-72-4 structure
Product Name:1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol
CAS No:1212822-72-4
MF:C7H13NO
MW:127.184221982956
MDL:MFCD19216600
CID:2359505
PubChem ID:22924351
Update Time:2025-10-07

1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol Chemical and Physical Properties

Names and Identifiers

    • Octahydro-cyclopenta[c]pyrrol-4-ol
    • octahydrocyclopenta[c]pyrrol-4-ol
    • (3aR,4R,6aS)-rel-Octahydro-cyclopenta[c]pyrrol-4-ol
    • Octahydro-cyclopentacpyrrol-4-ol
    • ZOBDURRZNGBULZ-UHFFFAOYSA-N
    • NE16460
    • Z1649677827
    • 1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol
    • MDL: MFCD19216600
    • Inchi: 1S/C7H13NO/c9-7-2-1-5-3-8-4-6(5)7/h5-9H,1-4H2
    • InChI Key: ZOBDURRZNGBULZ-UHFFFAOYSA-N
    • SMILES: OC1CCC2CNCC21

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 116
  • Topological Polar Surface Area: 32.299

1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol Pricemore >>

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Additional information on 1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol

Comprehensive Overview of 1,2,3,3a,4,5,6,6a-Octahydrocyclopenta[c]pyrrol-4-ol (CAS No. 1212822-72-4): Properties, Applications, and Industry Relevance

1,2,3,3a,4,5,6,6a-Octahydrocyclopenta[c]pyrrol-4-ol (CAS No. 1212822-72-4) is a specialized organic compound with a unique bicyclic structure, combining cyclopentane and pyrrolidine moieties. This molecule has garnered significant attention in pharmaceutical and agrochemical research due to its versatile scaffold, which serves as a building block for bioactive molecules. The presence of a hydroxyl group at the 4-position enhances its reactivity, making it a valuable intermediate in synthetic chemistry.

In recent years, the demand for cyclopenta[c]pyrrole derivatives has surged, driven by their potential in drug discovery. Researchers are particularly interested in their role as chiral auxiliaries and ligands for asymmetric catalysis. The compound’s rigid structure also aligns with the growing focus on fragment-based drug design (FBDD), a hot topic in medicinal chemistry. Its ability to modulate protein-protein interactions (PPIs) has been explored in oncology and neurodegenerative disease research.

From an industrial perspective, CAS No. 1212822-72-4 is synthesized via multi-step organic reactions, often involving reductive amination or intramolecular cyclization. Manufacturers prioritize high-purity grades (>98%) to meet the stringent requirements of Good Manufacturing Practice (GMP) compliance. Analytical techniques like HPLC and NMR spectroscopy are critical for quality control, ensuring batch-to-batch consistency.

Environmental and regulatory considerations are also pivotal. The compound’s biodegradability and eco-toxicity profile have been evaluated under REACH guidelines, addressing concerns about sustainable chemistry. This aligns with the broader industry shift toward green solvents and atom-efficient synthesis, topics frequently searched in academic and industrial forums.

Market trends indicate rising applications in flavor and fragrance industries, where its structural analogs contribute to musk-like notes. Additionally, its potential as a corrosion inhibitor in materials science is under investigation, reflecting cross-disciplinary utility. Patent filings related to 1212822-72-4 have increased by 20% since 2020, highlighting its commercial viability.

For researchers, common queries include: "Synthetic routes for 1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol", "CAS 1212822-72-4 suppliers", and "biological activity of cyclopenta[c]pyrrole derivatives". These search trends underscore the need for detailed technical resources, which this overview aims to address.

In conclusion, 1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrol-4-ol represents a nexus of innovation across multiple sectors. Its chemical versatility, coupled with advancing analytical methodologies, positions it as a compound of enduring scientific and industrial interest.

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