Cas no 1203799-41-0 (2-methyl-2,7-diazaspiro4.4nonan-1-one)

2-Methyl-2,7-diazaspiro[4.4]nonan-1-one is a spirocyclic compound featuring a diazaspiro core structure, which imparts unique steric and electronic properties. This heterocyclic scaffold is of significant interest in medicinal chemistry due to its rigid conformation, enhancing binding selectivity in drug design. The presence of both nitrogen atoms and a carbonyl group offers versatile reactivity for further functionalization, making it a valuable intermediate in the synthesis of bioactive molecules. Its spirocyclic framework contributes to improved metabolic stability and pharmacokinetic profiles in potential therapeutic agents. The compound is particularly useful in the development of CNS-targeting pharmaceuticals and enzyme inhibitors, where conformational restraint is critical for activity optimization.
2-methyl-2,7-diazaspiro4.4nonan-1-one structure
1203799-41-0 structure
Product Name:2-methyl-2,7-diazaspiro4.4nonan-1-one
CAS No:1203799-41-0
MF:C8H14N2O
MW:154.209561824799
MDL:MFCD16249896
CID:2105371
PubChem ID:55263207
Update Time:2025-10-22

2-methyl-2,7-diazaspiro4.4nonan-1-one Chemical and Physical Properties

Names and Identifiers

    • 2-methyl-2,7-Diazaspiro[4.4]nonan-1-one
    • CID 55263207
    • 2,7-Diazaspiro[4.4]nonan-1-one, 2-methyl-
    • 2-methyl-2,7-diazaspiro4.4nonan-1-one
    • MDL: MFCD16249896
    • Inchi: 1S/C8H14N2O/c1-10-5-3-8(7(10)11)2-4-9-6-8/h9H,2-6H2,1H3
    • InChI Key: MNGHKFUPDAFHRO-UHFFFAOYSA-N
    • SMILES: O=C1C2(CNCC2)CCN1C

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • Complexity: 193
  • Topological Polar Surface Area: 32.299

2-methyl-2,7-diazaspiro4.4nonan-1-one Pricemore >>

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Additional information on 2-methyl-2,7-diazaspiro4.4nonan-1-one

Comprehensive Overview of 2-methyl-2,7-diazaspiro[4.4]nonan-1-one (CAS No. 1203799-41-0)

The compound 2-methyl-2,7-diazaspiro[4.4]nonan-1-one (CAS No. 1203799-41-0) is a structurally unique spirocyclic molecule that has garnered significant attention in pharmaceutical and agrochemical research. Its diazaspiro core and methyl substitution make it a versatile intermediate for synthesizing bioactive compounds. Researchers are increasingly exploring its potential in drug discovery, particularly for targeting central nervous system (CNS) disorders and enzyme inhibition. The compound's spiro[4.4]nonane framework contributes to its conformational rigidity, enhancing binding affinity to biological targets.

In recent years, the demand for spirocyclic compounds like 2-methyl-2,7-diazaspiro[4.4]nonan-1-one has surged due to their applications in medicinal chemistry and material science. A growing trend in AI-driven drug design has highlighted the importance of such scaffolds for optimizing molecular properties and ADMET profiles. Users frequently search for terms like "spirocyclic synthesis," "diazaspiro derivatives," and "CAS 1203799-41-0 supplier," reflecting commercial and academic interest. This compound's heterocyclic nature also aligns with the search for "nitrogen-containing scaffolds" in high-throughput screening.

The synthetic routes to 2-methyl-2,7-diazaspiro[4.4]nonan-1-one often involve multicomponent reactions or ring-closing metathesis, topics frequently discussed in organic chemistry forums. Its ketone functionality allows further derivatization, making it a hotspot for "structure-activity relationship (SAR) studies." Environmental concerns have also driven searches for "green synthesis of spiro compounds," where this molecule serves as a case study for sustainable chemistry practices.

From a commercial perspective, CAS 1203799-41-0 is listed by specialty chemical vendors as a research-grade material, with purity levels critical for assay development. Its role in peptidomimetics and protease inhibitors has been explored in patent literature, linking it to trending topics like "anticancer drug candidates" and "neuroprotective agents." Analytical data, including NMR and HPLC profiles, are commonly requested by purchasers, emphasizing the need for rigorous quality control.

In conclusion, 2-methyl-2,7-diazaspiro[4.4]nonan-1-one represents a compelling example of how spiroheterocycles bridge academic research and industrial applications. Its relevance to fragment-based drug discovery and catalysis ensures continued interest, while SEO-optimized queries like "buy 1203799-41-0" underscore its market viability. Future studies may focus on its scalable production and biocompatibility, addressing both scientific and sustainability challenges.

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