Cas no 15742-68-4 (1,4-Bis(2,5-dimethylphenyl)methylbenzene)
1,4-Bis(2,5-dimethylphenyl)methylbenzene Chemical and Physical Properties
Names and Identifiers
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- 2-[[4-[(2,5-dimethylphenyl)methyl]phenyl]methyl]-1,4-dimethylbenzene
- 1,4-BIS[(2,5-DIMETHYLPHENYL)METHYL]BENZENE
- CTK4C9360
- 1,4-BIS-[(2,5-DIMETHYLPHENYL)-METHYL]-BENZENE
- KB-150784
- 2',5',2'',5''-Tetramethyl-1,4-dibenzylbenzol
- AG-E-06416
- 15742-68-4
- OAPLQKMSCKWYDX-UHFFFAOYSA-N
- 1,1'-[1,4-Phenylenebis(methylene)]bis(2,5-dimethylbenzene)
- Benzene, 1,4-bis[(2,5-dimethylphenyl)methyl]-
- DTXSID30634973
- 1,4-Bis(2,5-dimethylphenyl)methylbenzene
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- Inchi: 1S/C24H26/c1-17-5-7-19(3)23(13-17)15-21-9-11-22(12-10-21)16-24-14-18(2)6-8-20(24)4/h5-14H,15-16H2,1-4H3
- InChI Key: OAPLQKMSCKWYDX-UHFFFAOYSA-N
- SMILES: C(C1C=C(C)C=CC=1C)C1C=CC(=CC=1)CC1C=C(C)C=CC=1C
Computed Properties
- Exact Mass: 314.20358
- Monoisotopic Mass: 314.203450829g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 24
- Rotatable Bond Count: 4
- Complexity: 328
- 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: 7.2
- Topological Polar Surface Area: 0?2
Experimental Properties
- Density: 1.003
- Boiling Point: 447.3°C at 760 mmHg
- Flash Point: 222.4°C
- Refractive Index: 1.579
- PSA: 0
1,4-Bis(2,5-dimethylphenyl)methylbenzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B015869-2.5mg |
1,4-Bis[(2,5-dimethylphenyl)methyl]benzene |
15742-68-4 | 2.5mg |
$ 200.00 | 2022-06-07 | ||
| TRC | B015869-5mg |
1,4-Bis[(2,5-dimethylphenyl)methyl]benzene |
15742-68-4 | 5mg |
$ 370.00 | 2022-06-07 | ||
| TRC | B015869-10mg |
1,4-Bis[(2,5-dimethylphenyl)methyl]benzene |
15742-68-4 | 10mg |
$ 585.00 | 2022-06-07 |
1,4-Bis(2,5-dimethylphenyl)methylbenzene Related Literature
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1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
Additional information on 1,4-Bis(2,5-dimethylphenyl)methylbenzene
1,4-Bis(2,5-Dimethylphenyl)methylbenzene: A Comprehensive Overview
1,4-Bis(2,5-Dimethylphenyl)methylbenzene (CAS No. 15742-68-4) is a complex organic compound with a unique molecular structure that has garnered attention in various fields of chemistry and materials science. This compound belongs to the class of polycyclic aromatic hydrocarbons (PAHs), which are known for their stability and versatile applications. The molecule consists of three benzene rings, with two of them substituted at the 2 and 5 positions with methyl groups. This substitution pattern imparts distinct chemical and physical properties to the compound.
The molecular formula of 1,4-Bis(2,5-Dimethylphenyl)methylbenzene is C18H18, and its molecular weight is approximately 234 g/mol. The compound is characterized by its rigid planar structure due to the aromatic nature of the benzene rings. This rigidity contributes to its stability under various conditions. The compound is typically found in a crystalline solid state at room temperature and has a melting point of around 130°C.
Recent studies have focused on the synthesis and characterization of 1,4-Bis(2,5-Dimethylphenyl)methylbenzene to explore its potential applications in advanced materials. Researchers have employed various synthetic methods, including Friedel-Crafts alkylation and Suzuki coupling reactions, to efficiently synthesize this compound. These methods have been optimized to achieve high yields and purity levels.
One of the most promising applications of 1,4-Bis(2,5-Dimethylphenyl)methylbenzene lies in its use as a precursor for functional materials such as organic semiconductors and light-emitting diodes (LEDs). Its extended conjugated system allows for efficient charge transport properties, making it suitable for electronic devices. Recent advancements in nanotechnology have also explored the use of this compound in the development of graphene-like materials due to its aromaticity and structural stability.
In terms of environmental impact, 1,4-Bis(2,5-Dimethylphenyl)methylbenzene has been studied for its biodegradation potential. Research indicates that under aerobic conditions, the compound undergoes slow degradation due to its stable aromatic structure. However, further studies are required to fully understand its environmental fate and toxicity.
The compound's ability to form self-assembled monolayers (SAMs) has also been investigated for applications in surface chemistry and catalysis. SAMs formed by 1,4-Bis(2,5-Dimethylphenyl)methylbenzene exhibit high stability and can be used as templates for the synthesis of nanostructured materials.
In conclusion, 1,4-Bis(2,5-Dimethylphenyl)methylbenzene (CAS No. 15742-68-4) is a versatile organic compound with a wide range of potential applications in materials science and technology. Ongoing research continues to uncover new insights into its properties and uses, positioning it as a valuable component in the development of advanced functional materials.
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