Cas no 54118-73-9 (Methanone, (4-iodophenyl)(4-methoxyphenyl)-)

Methanone, (4-iodophenyl)(4-methoxyphenyl)-, is a diaryl ketone derivative characterized by the presence of an iodine substituent on one phenyl ring and a methoxy group on the other. This compound is of interest in synthetic organic chemistry due to its utility as an intermediate in the preparation of more complex molecules, particularly in pharmaceutical and materials science research. The iodine moiety offers a reactive site for further functionalization via cross-coupling reactions, while the methoxy group can influence electronic properties. Its well-defined structure and reactivity make it a valuable building block for targeted synthesis applications.
Methanone, (4-iodophenyl)(4-methoxyphenyl)- structure
54118-73-9 structure
Product Name:Methanone, (4-iodophenyl)(4-methoxyphenyl)-
CAS No:54118-73-9
MF:C14H11IO2
MW:338.140416383743
CID:355501
PubChem ID:22132674
Update Time:2025-11-02

Methanone, (4-iodophenyl)(4-methoxyphenyl)- Chemical and Physical Properties

Names and Identifiers

    • Methanone, (4-iodophenyl)(4-methoxyphenyl)-
    • (4-iodophenyl)-(4-methoxyphenyl)methanone
    • DTXSID00622685
    • (4-Iodophenyl)(4-methoxyphenyl)methanone
    • 4-Methoxyphenyl 4-iodophenyl ketone
    • RNVYWATVTGABNZ-UHFFFAOYSA-N
    • 54118-73-9
    • AMY27188
    • (4-Iodophenyl)[4-(methyloxy)phenyl]methanone
    • (4-iodophenyl)-(4-methoxyphenyl)-methanone
    • SCHEMBL3468539
    • (4-Iodo-phenyl)-(4-methoxy-phenyl)-methanone
    • Inchi: 1S/C14H11IO2/c1-17-13-8-4-11(5-9-13)14(16)10-2-6-12(15)7-3-10/h2-9H,1H3
    • InChI Key: RNVYWATVTGABNZ-UHFFFAOYSA-N
    • SMILES: IC1C=CC(=CC=1)C(C1C=CC(=CC=1)OC)=O

Computed Properties

  • Exact Mass: 337.97993
  • Monoisotopic Mass: 337.98038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3
  • Complexity: 251
  • 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: 3.9
  • Topological Polar Surface Area: 26.3?2

Experimental Properties

  • PSA: 26.3

Methanone, (4-iodophenyl)(4-methoxyphenyl)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
A2B Chem LLC
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Methanone, (4-iodophenyl)(4-methoxyphenyl)-
54118-73-9 95%-98%
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$289.00 2024-04-19
A2B Chem LLC
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Methanone, (4-iodophenyl)(4-methoxyphenyl)-
54118-73-9 95%-98%
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Methanone, (4-iodophenyl)(4-methoxyphenyl)- Related Literature

Additional information on Methanone, (4-iodophenyl)(4-methoxyphenyl)-

Comprehensive Overview of Methanone, (4-iodophenyl)(4-methoxyphenyl)- (CAS No. 54118-73-9)

Methanone, (4-iodophenyl)(4-methoxyphenyl)-, with the CAS number 54118-73-9, is a specialized organic compound that has garnered significant attention in pharmaceutical and material science research. This compound, often referred to by its systematic name, belongs to the class of aromatic ketones, which are pivotal intermediates in synthesizing advanced materials and bioactive molecules. Its unique structure, featuring both iodo and methoxy functional groups, makes it a versatile building block for cross-coupling reactions and photochemical applications.

In recent years, the demand for iodinated aromatic compounds like Methanone, (4-iodophenyl)(4-methoxyphenyl)- has surged due to their role in drug discovery and organic electronics. Researchers are particularly interested in its potential as a photoinitiator or ligand in catalytic systems. The compound’s electron-rich and electron-deficient regions enable it to participate in diverse chemical transformations, aligning with trends in green chemistry and sustainable synthesis.

One of the most frequently searched questions about CAS 54118-73-9 revolves around its synthetic applications. For instance, how does this compound facilitate Suzuki-Miyaura coupling or Ullmann reactions? The answer lies in its 4-iodophenyl moiety, which acts as an excellent leaving group in metal-catalyzed cross-coupling reactions. Additionally, the 4-methoxyphenyl group enhances solubility and stability, making it ideal for high-throughput screening in medicinal chemistry.

Another hot topic is the compound’s role in advanced material science. With the rise of OLEDs (Organic Light-Emitting Diodes) and photovoltaic cells, Methanone, (4-iodophenyl)(4-methoxyphenyl)- is explored as a precursor for π-conjugated systems. Its ability to absorb UV light and transfer energy efficiently positions it as a candidate for optoelectronic devices. This aligns with global interest in renewable energy and smart materials.

From a safety and handling perspective, CAS 54118-73-9 is typically handled under standard laboratory conditions. While not classified as hazardous, its iodine component necessitates precautions to avoid unnecessary exposure. Researchers often inquire about its storage conditions (e.g., light-sensitive, inert atmosphere) and compatibility with common solvents, which are critical for experimental reproducibility.

In summary, Methanone, (4-iodophenyl)(4-methoxyphenyl)- (54118-73-9) is a multifaceted compound bridging pharmaceutical innovation and material engineering. Its relevance in catalysis, optoelectronics, and drug design ensures its continued prominence in scientific literature. As industries pivot toward sustainable technologies, this compound’s adaptability will likely fuel further breakthroughs.

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