Cas no 1187173-73-4 (2,9-Diazaspiro[5.5]undecan-1-one hydrochloride)

2,9-Diazaspiro[5.5]undecan-1-one hydrochloride is a bicyclic spiro compound featuring a diazaspiro core structure, which is of significant interest in medicinal chemistry and pharmaceutical research. The hydrochloride salt enhances its solubility and stability, making it suitable for synthetic applications. This scaffold is particularly valuable as a building block for the development of bioactive molecules, including potential therapeutics targeting neurological and metabolic disorders. Its rigid spirocyclic framework offers conformational restraint, which can improve binding affinity and selectivity in drug design. The compound’s high purity and well-defined structure ensure reproducibility in research settings, supporting its use in lead optimization and molecular exploration.
2,9-Diazaspiro[5.5]undecan-1-one hydrochloride structure
1187173-73-4 structure
Product Name:2,9-Diazaspiro[5.5]undecan-1-one hydrochloride
CAS No:1187173-73-4
MF:C9H17ClN2O
MW:204.697081327438
MDL:MFCD08461145
CID:1070470
PubChem ID:45074288
Update Time:2025-06-08

2,9-Diazaspiro[5.5]undecan-1-one hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride
    • EN300-7416391
    • 1187173-73-4
    • AKOS024015348
    • MFCD08461145
    • ALBB-022298
    • 2,9-Diazaspiro[5.5]undecan-1-one hydrogen chloride
    • DTXSID10662895
    • PB26375
    • CS-0052122
    • 2,9-diazaspiro[5.5]undecan-1-one;hydrochloride
    • AKOS032949972
    • DB-329715
    • SYMGZOBPONIUTK-UHFFFAOYSA-N
    • SY112703
    • SCHEMBL2026185
    • AS-38379
    • 2,9-DIAZASPIRO[5.5]UNDECAN-1-ONE HCL
    • 2,9-Diazaspiro[5.5]undecan-1-one--hydrogen chloride (1/1)
    • MDL: MFCD08461145
    • Inchi: 1S/C9H16N2O.ClH/c12-8-9(2-1-5-11-8)3-6-10-7-4-9;/h10H,1-7H2,(H,11,12);1H
    • InChI Key: SYMGZOBPONIUTK-UHFFFAOYSA-N
    • SMILES: Cl.O=C1C2(CCNCC2)CCCN1

Computed Properties

  • Exact Mass: 204.1029409g/mol
  • Monoisotopic Mass: 204.1029409g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 185
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 41.1?2

2,9-Diazaspiro[5.5]undecan-1-one hydrochloride Pricemore >>

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Additional information on 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride

2,9-Diazaspiro[5.5]undecan-1-one hydrochloride (CAS No. 1187173-73-4)

The compound 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride, identified by the CAS registry number 1187173-73-4, is a spirocyclic compound with significant potential in various chemical and pharmaceutical applications. This molecule belongs to the class of diazaspiro compounds, which have garnered attention due to their unique structural features and promising biological activities.

Spiro compounds are characterized by the presence of two rings connected by a single atom, often leading to complex three-dimensional structures that can mimic natural product frameworks. In the case of 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride, the spiro arrangement involves a 5-membered ring fused with another 5-membered ring, creating a rigid and compact structure ideal for various chemical reactions and biological interactions.

Recent studies have highlighted the importance of spirocyclic compounds in drug discovery, particularly in the development of kinase inhibitors and other therapeutic agents. The presence of nitrogen atoms in the spiro system of 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride introduces additional functional groups that can enhance its binding affinity to target proteins, making it a valuable candidate for further exploration in medicinal chemistry.

The synthesis of 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride involves multi-step organic reactions, including cyclization and ring-forming processes that require precise control over reaction conditions to achieve high yields and purity. Researchers have employed various strategies such as microwave-assisted synthesis and catalytic methods to optimize the production of this compound.

In terms of biological activity, 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride has shown potential as an inhibitor of several enzymes involved in cellular signaling pathways, which are often implicated in diseases such as cancer and neurodegenerative disorders. Preclinical studies suggest that this compound exhibits selective binding to its target proteins without significant off-target effects, indicating its potential as a lead compound for drug development.

Moreover, the spirocyclic structure of 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride provides opportunities for further functionalization to enhance its pharmacokinetic properties, such as bioavailability and metabolic stability. This versatility makes it a promising scaffold for designing next-generation therapeutics.

In conclusion, 2,9-Diazaspiro[5.5]undecan-1-one hydrochloride (CAS No. 1187173-73-4) represents a valuable addition to the arsenal of spirocyclic compounds with applications in drug discovery and chemical synthesis. Its unique structure and promising biological profile underscore its potential as a key player in advancing medical research and therapeutic development.

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