Cas no 74606-53-4 (N-Noratherosperminine)

N-Noratherosperminine structure
N-Noratherosperminine structure
Product Name:N-Noratherosperminine
CAS No:74606-53-4
MF:C19H21NO2
MW:295.37554526329
CID:2002130
PubChem ID:10957406
Update Time:2025-07-17

N-Noratherosperminine Chemical and Physical Properties

Names and Identifiers

    • N-Noratherosperminine
    • Noratherosperminine
    • HY-N12157
    • 74606-53-4
    • AKOS040763686
    • CS-0892551
    • DA-76253
    • Theatre-in-the-round
    • Inchi: 1S/C19H21NO2/c1-20-11-10-14-12-17(21-2)19(22-3)18-15-7-5-4-6-13(15)8-9-16(14)18/h4-9,12,20H,10-11H2,1-3H3
    • InChI Key: BRMNMGRFCCRFNA-UHFFFAOYSA-N
    • SMILES: O(C)C1C(=CC(CCNC)=C2C=CC3C=CC=CC=3C2=1)OC

Computed Properties

  • Exact Mass: 295.157228913g/mol
  • Monoisotopic Mass: 295.157228913g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 5
  • Complexity: 348
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4.2
  • Topological Polar Surface Area: 30.5?2

N-Noratherosperminine Pricemore >>

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Additional information on N-Noratherosperminine

Exploring N-Noratherosperminine (CAS No. 74606-53-4): A Comprehensive Review of Its Properties and Applications

N-Noratherosperminine (CAS No. 74606-53-4) is a naturally occurring alkaloid that has garnered significant attention in recent years due to its unique chemical structure and potential applications in various fields. This compound belongs to the aporphine class of alkaloids, which are known for their diverse biological activities. Researchers and industry professionals are increasingly interested in N-Noratherosperminine for its potential therapeutic properties, making it a hot topic in both academic and commercial circles.

The chemical structure of N-Noratherosperminine features a tetracyclic framework, which is characteristic of aporphine alkaloids. This structural motif is often associated with interactions with biological targets, particularly in the central nervous system. Recent studies have explored its potential as a modulator of neurotransmitter systems, sparking interest in its possible applications in neurological research. The compound's CAS number 74606-53-4 serves as a unique identifier in chemical databases, facilitating research and regulatory compliance.

In the context of current scientific trends, N-Noratherosperminine aligns with the growing interest in plant-derived compounds and their potential health benefits. The global market for natural products is expanding rapidly, with consumers increasingly seeking alternatives to synthetic compounds. This trend has led to more research into alkaloids like N-Noratherosperminine, particularly regarding their bioavailability and metabolic pathways. Scientists are particularly interested in how this compound compares to other aporphine alkaloids in terms of stability and biological activity.

From a technical perspective, the synthesis and isolation of N-Noratherosperminine present interesting challenges for organic chemists. The compound's specific stereochemistry and functional groups require specialized techniques for purification and characterization. Advanced analytical methods such as HPLC-MS and NMR spectroscopy are typically employed to verify the identity and purity of CAS 74606-53-4 samples. These analytical challenges contribute to the compound's significance in methodological development within natural product chemistry.

The potential applications of N-Noratherosperminine extend beyond basic research. In the pharmaceutical industry, there is growing interest in exploring its structure-activity relationships to develop novel compounds with improved pharmacological profiles. The compound's molecular framework serves as an interesting scaffold for medicinal chemistry modifications. Furthermore, its natural origin makes it an attractive candidate for development in markets that favor plant-based ingredients.

Quality control and standardization of N-Noratherosperminine preparations are critical aspects for researchers and manufacturers working with this compound. The variability in natural sources and extraction methods necessitates rigorous analytical protocols to ensure consistency. Reference standards of CAS 74606-53-4 are essential for these quality control processes, highlighting the importance of reliable chemical suppliers in this niche market.

Environmental considerations are also coming to the forefront in discussions about N-Noratherosperminine production. Sustainable sourcing of plant materials and eco-friendly extraction methods are becoming increasingly important to meet both regulatory requirements and consumer expectations. These considerations add another layer of complexity to the study and commercialization of this interesting alkaloid.

Looking to the future, research on N-Noratherosperminine is likely to focus on several key areas. These include detailed pharmacological profiling, structure-optimization studies, and investigation of potential synergistic effects with other natural compounds. The compound's CAS number 74606-53-4 will continue to serve as an important reference point as this research progresses and as regulatory frameworks for natural products continue to evolve worldwide.

For researchers entering this field, understanding the physicochemical properties of N-Noratherosperminine is essential. The compound's solubility characteristics, stability under various conditions, and compatibility with different formulation approaches are all important factors that influence its potential applications. These practical considerations complement the more theoretical aspects of its biological activity and mechanism of action.

In conclusion, N-Noratherosperminine (CAS No. 74606-53-4) represents an intriguing subject of study at the intersection of natural product chemistry and potential therapeutic development. Its unique structural features and biological activities make it a compound of continuing interest to researchers across multiple disciplines. As scientific techniques advance and market trends evolve, our understanding and utilization of this alkaloid are likely to expand in exciting new directions.

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