Cas no 39148-55-5 (biphenyl-4-yl(4-methylphenyl)methanone)

Biphenyl-4-yl(4-methylphenyl)methanone is a high-purity organic compound primarily utilized as an intermediate in pharmaceutical and specialty chemical synthesis. Its biphenyl and methylphenyl ketone structure offers versatility in cross-coupling reactions and functional group transformations. The compound exhibits excellent thermal stability and solubility in common organic solvents, facilitating its integration into complex synthetic pathways. Its well-defined crystalline form ensures consistent reactivity and ease of handling in laboratory and industrial settings. As a building block, it enables precise modifications for applications in materials science, agrochemicals, and drug development. Rigorous quality control guarantees high batch-to-batch reproducibility, meeting stringent research and production requirements.
biphenyl-4-yl(4-methylphenyl)methanone structure
39148-55-5 structure
Product Name:biphenyl-4-yl(4-methylphenyl)methanone
CAS No:39148-55-5
MF:C20H16O
MW:272.340445518494
MDL:MFCD00623207
CID:1499333
PubChem ID:217661
Update Time:2025-08-05

biphenyl-4-yl(4-methylphenyl)methanone Chemical and Physical Properties

Names and Identifiers

    • biphenyl-4-yl(4-methylphenyl)methanone
    • Biphenyl-4-yl-p-tolyl-methanone
    • 4-Methyl-4'-phenylbenzophenone
    • Benzophenone, 4-methyl-4'-phenyl-
    • starbld0006694
    • [1,1'-Biphenyl]-4-yl(p-tolyl)methanone
    • SCHEMBL2450704
    • SY284392
    • ([1,1'-Biphenyl]-4-yl)(4-methylphenyl)methanone
    • DTXSID40959947
    • BRN 2457167
    • Methanone, (1,1'-biphenyl-4-yl)(4-methylphenyl)-
    • {[1,1'-BIPHENYL]-4-YL}(4-METHYLPHENYL)METHANONE
    • 39148-55-5
    • 3-07-00-02749 (Beilstein Handbook Reference)
    • A828542
    • BS-47121
    • SR-01000389188-1
    • 4-Biphenylyl(p-tolyl)methanone
    • AKOS000728027
    • (4-methylphenyl)-(4-phenylphenyl)methanone
    • AB01330959-02
    • SR-01000389188
    • MFCD00623207
    • NCGC00338728-01
    • MDL: MFCD00623207
    • Inchi: 1S/C20H16O/c1-15-7-9-18(10-8-15)20(21)19-13-11-17(12-14-19)16-5-3-2-4-6-16/h2-14H,1H3
    • InChI Key: FHXOSEAUHPYUAO-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC(C)=CC=1)C1C=CC(=CC=1)C1C=CC=CC=1

Computed Properties

  • Exact Mass: 272.12018
  • Monoisotopic Mass: 272.120115130g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 3
  • Complexity: 326
  • 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: 5.3
  • Topological Polar Surface Area: 17.1?2

Experimental Properties

  • PSA: 17.07

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biphenyl-4-yl(4-methylphenyl)methanone Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:39148-55-5)biphenyl-4-yl(4-methylphenyl)methanone
Order Number:A1220743
Stock Status:in Stock
Quantity:500g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 19:26
Price ($):284

Additional information on biphenyl-4-yl(4-methylphenyl)methanone

Biphenyl-4-yl(4-methylphenyl)methanone: A Comprehensive Overview

Biphenyl-4-yl(4-methylphenyl)methanone, also known by its CAS number 39148-55-5, is a compound of significant interest in the fields of organic chemistry and materials science. This compound, characterized by its unique structure, has garnered attention due to its potential applications in various industries. The molecule consists of two aromatic rings connected by a methanone group, with one ring substituted at the para position by a methyl group. This structural arrangement imparts distinctive chemical and physical properties to the compound.

Recent studies have highlighted the importance of biphenyl derivatives in the development of advanced materials. For instance, researchers have explored the use of biphenyl-containing compounds in the synthesis of high-performance polymers and organic semiconductors. The presence of the methanone group in biphenyl-4-yl(4-methylphenyl)methanone introduces additional functional versatility, making it a valuable precursor in organic synthesis.

The synthesis of biphenyl-4-yl(4-methylphenyl)methanone typically involves nucleophilic aromatic substitution or coupling reactions. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing production costs and environmental impact. For example, the use of palladium-catalyzed cross-coupling reactions has been reported to enhance the yield and purity of this compound.

In terms of applications, biphenyl derivatives are increasingly being utilized in pharmaceutical research. The compound's ability to act as a chiral auxiliary or a building block for complex molecules has made it a valuable tool in drug discovery. Recent studies have demonstrated its potential as an intermediate in the synthesis of bioactive compounds with anti-inflammatory and anticancer properties.

The physical properties of biphenyl-4-yl(4-methylphenyl)methanone are also worth noting. Its melting point and solubility characteristics make it suitable for use in various chemical processes. Additionally, its thermal stability has been studied extensively, with recent research indicating its suitability for high-temperature applications.

In conclusion, biphenyl-4-yl(4-methylphenyl)methanone (CAS No: 39148-55-5) is a versatile compound with a wide range of applications across multiple disciplines. Its unique structure, combined with recent advancements in synthetic methodologies, positions it as a key player in modern chemical research and industry.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:39148-55-5)biphenyl-4-yl(4-methylphenyl)methanone
A1220743
Purity:99%
Quantity:500g
Price ($):284
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