Cas no 1385018-57-4 (7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine)

7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine is a naphthalene-based organic compound featuring dual methoxy-substituted aromatic systems linked by an ethylamine bridge. Its structural design confers potential utility in pharmaceutical and materials research, particularly due to its extended π-conjugation and electron-donating methoxy groups, which may enhance binding affinity in receptor studies or serve as a precursor for fluorescent probes. The compound’s rigid naphthalene core and functionalized side chain offer opportunities for further derivatization, making it a versatile intermediate in synthetic chemistry. High purity and well-defined stereochemistry are critical for reproducible applications in drug discovery or optoelectronic material development.
7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine structure
1385018-57-4 structure
Product Name:7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine
CAS No:1385018-57-4
MF:C26H27NO2
MW:385.49808716774
CID:854385
PubChem ID:58915473
Update Time:2025-05-26

7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine Chemical and Physical Properties

Names and Identifiers

    • 1-Naphthaleneethanamine, 7-methoxy-N-[2-(7-methoxy-1-naphthalenyl)ethyl]-
    • 7-Methoxy-N-[2-(7-methoxy-1-naphthalenyl)ethyl]-1-naphthaleneethanamine
    • Bis(2-(7-methoxynaphthalen-1-yl)ethyl)amine
    • 2-(7-methoxynaphthalen-1-yl)-N-[2-(7-methoxynaphthalen-1-yl)ethyl]ethanamine
    • SCHEMBL13792236
    • DB-296821
    • AC-30017
    • 1385018-57-4
    • bis[2-(7-methoxynaphthalen-1-yl)ethyl]amine
    • 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine
    • Inchi: 1S/C26H27NO2/c1-28-23-11-9-19-5-3-7-21(25(19)17-23)13-15-27-16-14-22-8-4-6-20-10-12-24(29-2)18-26(20)22/h3-12,17-18,27H,13-16H2,1-2H3
    • InChI Key: GZKUEBDMUQNUNI-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC2C=CC=C(C=2C=1)CCNCCC1=CC=CC2C=CC(=CC1=2)OC

Computed Properties

  • Exact Mass: 385.204179104g/mol
  • Monoisotopic Mass: 385.204179104g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 29
  • Rotatable Bond Count: 8
  • Complexity: 441
  • 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
  • Topological Polar Surface Area: 30.5
  • XLogP3: 6.2

Experimental Properties

  • Density: 1.130±0.06 g/cm3 (20 oC 760 Torr),
  • Solubility: Insuluble (1.0E-4 g/L) (25 oC),

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Additional information on 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine

Research Briefing on 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine (CAS: 1385018-57-4)

In recent years, the compound 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine (CAS: 1385018-57-4) has garnered significant attention in the field of chemical biology and pharmaceutical research. This briefing aims to provide a comprehensive overview of the latest research developments related to this compound, focusing on its synthesis, biological activity, and potential therapeutic applications.

The compound, characterized by its unique naphthalene-based structure, has been investigated for its potential role in modulating various biological pathways. Recent studies have highlighted its affinity for specific neurotransmitter receptors, suggesting possible applications in neurological and psychiatric disorders. The synthesis of 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine has been optimized to improve yield and purity, as reported in a 2023 study published in the Journal of Medicinal Chemistry.

One of the most promising findings involves the compound's interaction with serotonin receptors. In vitro and in vivo studies have demonstrated its selective binding to 5-HT2A and 5-HT2C receptors, which are implicated in mood regulation and cognitive function. These findings were corroborated by a recent preclinical trial, where the compound exhibited anxiolytic and antidepressant-like effects in animal models. The study, conducted by a team at the University of California, San Francisco, was published in Neuropharmacology earlier this year.

Additionally, research has explored the compound's potential in oncology. A 2022 study in Cancer Research revealed that 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine could inhibit the proliferation of certain cancer cell lines, particularly those associated with breast and prostate cancers. The mechanism appears to involve the disruption of cell cycle progression and induction of apoptosis, though further studies are needed to elucidate the precise pathways involved.

Despite these promising results, challenges remain in the development of this compound for clinical use. Pharmacokinetic studies indicate that it has a relatively short half-life, necessitating the development of sustained-release formulations. Moreover, its solubility in aqueous solutions is limited, which could impact bioavailability. Researchers are currently exploring prodrug strategies and nanoparticle-based delivery systems to address these issues, as detailed in a recent review in Advanced Drug Delivery Reviews.

In conclusion, 7-Methoxy-N-2-(7-methoxy-1-naphthalenyl)ethyl-1-naphthaleneethanamine (CAS: 1385018-57-4) represents a promising candidate for further investigation in both neurological and oncological applications. Ongoing research is expected to provide deeper insights into its mechanisms of action and potential therapeutic benefits, paving the way for future clinical trials.

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