Cas no 39148-55-5 (biphenyl-4-yl(4-methylphenyl)methanone)
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
biphenyl-4-yl(4-methylphenyl)methanone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1192060-500g |
4-Biphenylyl(p-tolyl)methanone |
39148-55-5 | 95% | 500g |
$330 | 2023-09-03 | |
| Aaron | AR01GCBM-500g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 500g |
$128.00 | 2025-02-11 | |
| 1PlusChem | 1P01GC3A-25g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 25g |
$7.00 | 2024-05-03 | |
| 1PlusChem | 1P01GC3A-100g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 100g |
$24.00 | 2024-05-03 | |
| 1PlusChem | 1P01GC3A-500g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 500g |
$112.00 | 2024-05-03 | |
| Aaron | AR01GCBM-5g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 5g |
$5.00 | 2025-02-11 | |
| Aaron | AR01GCBM-25g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 25g |
$8.00 | 2025-02-11 | |
| Aaron | AR01GCBM-100g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 100g |
$26.00 | 2025-02-11 | |
| A2B Chem LLC | AY40982-25g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 25g |
$6.00 | 2024-04-20 | |
| A2B Chem LLC | AY40982-100g |
4-Methyl-4-phenylbenzophenone |
39148-55-5 | 98% | 100g |
$22.00 | 2024-04-20 |
biphenyl-4-yl(4-methylphenyl)methanone Suppliers
biphenyl-4-yl(4-methylphenyl)methanone Related Literature
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
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Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
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Philipp Traber,Stephan Kupfer,Stefanie Gr?fe,Isabelle Baussanne,Martine Demeunynck,Jean-Marie Mouesca,Serge Gambarelli,Vincent Artero,Murielle Chavarot-Kerlidou Chem. Sci., 2018,9, 4152-4159
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.
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