Cas no 1770-82-7 (4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl)
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl Chemical and Physical Properties
Names and Identifiers
-
- 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl
- 1-iodo-4-[4-[4-(4-iodophenyl)phenyl]phenyl]benzene
- NULL
- 4'',1''']quaterphenyl
- DTXSID10727216
- 4/'/',1/'/'/']quaterphenyl
- 4,4'''-Diiodo-[1,1';4',1'';4'',1''']quaterphenyl
- BAA77082
- 1770-82-7
- AMY27126
- 1~4~,4~4~-Diiodo-1~1~,2~1~:2~4~,3~1~:3~4~,4~1~-quaterphenyl
- SCHEMBL2069523
-
- Inchi: 1S/C24H16I2/c25-23-13-9-21(10-14-23)19-5-1-17(2-6-19)18-3-7-20(8-4-18)22-11-15-24(26)16-12-22/h1-16H
- InChI Key: CPORZGXQUSQYOH-UHFFFAOYSA-N
- SMILES: IC1C=CC(=CC=1)C1C=CC(=CC=1)C1C=CC(C2C=CC(=CC=2)I)=CC=1
Computed Properties
- Exact Mass: 557.93415g/mol
- Monoisotopic Mass: 557.93415g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 26
- Rotatable Bond Count: 3
- Complexity: 364
- 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: 8.1
- Topological Polar Surface Area: 0?2
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019117864-1g |
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl |
1770-82-7 | 95% | 1g |
507.18 USD | 2021-06-16 | |
| Crysdot LLC | CD12131967-1g |
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl |
1770-82-7 | 95+% | 1g |
$581 | 2024-07-24 |
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl Related Literature
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Max Attwood,Hiroki Akutsu,Lee Martin,Toby J. Blundell,Pierre Le Maguere,Scott S. Turner Dalton Trans., 2021,50, 11843-11851
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
-
Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
Additional information on 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl
4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl (CAS No. 1770-82-7): A Versatile Organic Semiconductor for Advanced Applications
In the realm of organic electronics and advanced materials, 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl (CAS No. 1770-82-7) has emerged as a compound of significant interest. This iodinated quaterphenyl derivative is renowned for its unique structural properties, making it a valuable building block in the synthesis of high-performance organic semiconductors, liquid crystals, and optoelectronic devices. Researchers and industries alike are increasingly exploring its potential, driven by the growing demand for sustainable and efficient materials in fields such as flexible electronics, OLED displays, and photovoltaic cells.
The molecular structure of 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl features a linear arrangement of four phenyl rings, with iodine atoms strategically positioned at the terminal ends. This design enhances its electron-withdrawing capabilities, which is critical for tuning the electronic properties of conjugated systems. Such characteristics are highly sought after in the development of organic field-effect transistors (OFETs) and light-emitting diodes (LEDs), where charge transport and luminescence efficiency are paramount.
One of the most compelling aspects of this compound is its role in sustainable technology. As the world shifts toward greener alternatives, 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl offers a pathway to reduce reliance on traditional silicon-based electronics. Its compatibility with solution-processable techniques, such as inkjet printing, aligns with the industry's push for low-cost manufacturing and scalable production. This has sparked a surge in research publications and patent filings, reflecting its potential to revolutionize next-generation devices.
Beyond electronics, this compound has found applications in advanced materials science. Its ability to form stable crystalline phases makes it a candidate for molecular self-assembly and nanostructured materials. Scientists are also investigating its use in sensors and catalysts, leveraging its iodine-rich structure for enhanced reactivity and selectivity. These diverse applications underscore its versatility and the breadth of opportunities it presents.
For those seeking to understand the synthesis of 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl, the process typically involves palladium-catalyzed cross-coupling reactions, which are well-documented in organic chemistry literature. The compound's high purity and stability under ambient conditions further contribute to its appeal for industrial and academic use. Additionally, its solubility in common organic solvents simplifies handling and integration into various formulations.
As the demand for innovative materials continues to rise, 4,4'''-Diiodo-1,1':4',1'':4'',1'''-quaterphenyl stands out as a key player in the transition toward more efficient and environmentally friendly technologies. Its multifaceted applications and robust chemical properties position it as a cornerstone in the future of organic electronics and material science. For researchers and manufacturers alike, this compound represents a promising avenue for innovation and discovery.
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