Cas no 71186-85-1 ((3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone)

(3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone structure
71186-85-1 structure
Product Name:(3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone
CAS No:71186-85-1
MF:C15H13FO3
MW:260.260328054428
CID:1032288
PubChem ID:11076177
Update Time:2025-11-02

(3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone Chemical and Physical Properties

Names and Identifiers

    • (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone
    • (3,4-dimethoxyphenyl)-(4-fluorophenyl)methanone
    • 3,4-dimethoxy-4'-fluorobenzophenone
    • 3,4-Dimethoxy-4'-fluoro-benzophenone
    • AK122873
    • ST4135317
    • STK271159
    • SureCN3973496
    • 71186-85-1
    • ZAWIHPQSOJGMOW-UHFFFAOYSA-N
    • CS-0357177
    • DTXSID60454383
    • SCHEMBL3973496
    • AKOS005216391
    • DB-327715
    • Inchi: 1S/C15H13FO3/c1-18-13-8-5-11(9-14(13)19-2)15(17)10-3-6-12(16)7-4-10/h3-9H,1-2H3
    • InChI Key: ZAWIHPQSOJGMOW-UHFFFAOYSA-N
    • SMILES: FC1C=CC(=CC=1)C(C1C=CC(=C(C=1)OC)OC)=O

Computed Properties

  • Exact Mass: 260.08489
  • Monoisotopic Mass: 260.08487243g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 4
  • Complexity: 300
  • 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: 3.5
  • Topological Polar Surface Area: 35.5?2

Experimental Properties

  • PSA: 35.53

(3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone Pricemore >>

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Additional information on (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone

Comprehensive Overview of (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone (CAS No. 71186-85-1)

(3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone, with the CAS number 71186-85-1, is a specialized organic compound that has garnered significant attention in pharmaceutical and material science research. This methanone derivative features a unique molecular structure combining dimethoxy and fluorophenyl groups, making it a valuable intermediate in synthetic chemistry. Researchers and industry professionals often search for high-purity 71186-85-1 or synthesis methods for (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone, reflecting its growing relevance in advanced applications.

The compound’s structural attributes, including its aromatic ketone backbone, contribute to its utility in designing bioactive molecules. Recent studies highlight its potential role in developing central nervous system (CNS) targeting agents, aligning with the rising demand for neurological disorder therapeutics. Queries like "role of 71186-85-1 in drug discovery" or "fluorophenyl methanone applications" underscore its intersection with cutting-edge medical research. Additionally, its thermal stability and solubility profile make it a candidate for advanced material formulations, particularly in OLEDs and polymeric coatings.

From a synthetic perspective, CAS 71186-85-1 is often synthesized via Friedel-Crafts acylation, a topic frequently explored in academic forums. Optimizing yield and purity of (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone remains a key focus, with researchers sharing protocols for green chemistry adaptations to reduce environmental impact. This aligns with broader trends toward sustainable chemical production, a hot topic in 2024. Searches for "eco-friendly synthesis of fluorophenyl ketones" or "scalable production of 71186-85-1" reflect this shift.

Analytical characterization of 71186-85-1 typically involves HPLC, NMR, and mass spectrometry, ensuring compliance with pharmaceutical-grade standards. The compound’s chromatographic behavior and spectral data are well-documented, aiding quality control in industrial settings. Users often seek "analytical methods for 3,4-dimethoxyphenyl ketones" or "CAS 71186-85-1 purity testing," highlighting the need for reliable technical resources.

Beyond laboratories, (3,4-Dimethoxyphenyl)(4-fluorophenyl)methanone sparks interest in intellectual property (IP) landscapes. Patent databases reveal its inclusion in novel drug formulations and material science patents, driving queries like "71186-85-1 patent applications." Its multidisciplinary applications—from medicinal chemistry to electronics—position it as a compound with enduring scientific and commercial value.

In summary, CAS No. 71186-85-1 exemplifies the convergence of innovation and practical utility in modern chemistry. Whether for drug development, material engineering, or sustainable synthesis, this compound continues to inspire research and industrial adoption. As demand grows, so does the importance of accessible, accurate information—making this overview a vital resource for stakeholders across sectors.

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