Cas no 258-14-0 (Quinoxalino[2,3-b]quinoxaline)
Quinoxalino[2,3-b]quinoxaline Chemical and Physical Properties
Names and Identifiers
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- Quinoxalino[2,3-b]quinoxaline
- 5,6,11,12-Tetraazanaphthacene
- NSC 129574
- NSC 667257
- Quinoxaloquinoxaline
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- MDL: MFCD13194780
- Inchi: 1S/C14H8N4/c1-2-6-10-9(5-1)15-13-14(16-10)18-12-8-4-3-7-11(12)17-13/h1-8H
- InChI Key: RKOODWXAVAEOQW-UHFFFAOYSA-N
- SMILES: N1C2C=CC=CC=2N=C2C=1N=C1C=CC=CC1=N2
Computed Properties
- Exact Mass: 232.07504
Experimental Properties
- PSA: 51.56
Quinoxalino[2,3-b]quinoxaline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | Q856388-5g |
Quinoxalino[2,3-b]quinoxaline |
258-14-0 | 98% | 5g |
¥12,000.00 | 2022-08-31 | |
| eNovation Chemicals LLC | D626896-5g |
Isopropyl tri(dioctylphosphate)titanate |
258-14-0 | 97% | 5g |
$3381 | 2024-05-23 | |
| eNovation Chemicals LLC | D626896-5g |
Isopropyl tri(dioctylphosphate)titanate |
258-14-0 | 97% | 5g |
$3381 | 2025-02-19 | |
| eNovation Chemicals LLC | D626896-5g |
Isopropyl tri(dioctylphosphate)titanate |
258-14-0 | 97% | 5g |
$3381 | 2025-02-27 |
Quinoxalino[2,3-b]quinoxaline Related Literature
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1. Cyclisation chemistry of 4H-1,2,6-thiadiazinesPanayiotis A. Koutentis,Charles W. Rees J. Chem. Soc. Perkin Trans. 1 2000 2601
Additional information on Quinoxalino[2,3-b]quinoxaline
Quinoxalino[2,3-b]quinoxaline: A Comprehensive Overview
Quinoxalino[2,3-b]quinoxaline, also known by its CAS number 258-14-0, is a fascinating compound with a unique chemical structure that has garnered significant attention in the scientific community. This compound belongs to the class of polycyclic aromatic hydrocarbons (PAHs), which are characterized by their stable aromatic systems and versatile applications. Recent advancements in materials science and organic chemistry have highlighted the potential of Quinoxalino[2,3-b]quinoxaline in various fields, including electronics, optoelectronics, and drug delivery systems.
The molecular structure of Quinoxalino[2,3-b]quinoxaline consists of two fused quinoxaline rings, creating a rigid and planar framework. This structural feature contributes to its exceptional electronic properties, such as high electron mobility and strong absorption in the visible spectrum. Researchers have exploited these properties to develop advanced materials for organic light-emitting diodes (OLEDs) and photovoltaic devices. For instance, a study published in *Nature Communications* demonstrated that incorporating Quinoxalino[2,3-b]quinoxaline into OLEDs significantly enhances their efficiency and stability due to its ability to facilitate efficient charge transport.
One of the most promising applications of Quinoxalino[2,3-b]quinoxaline lies in its use as a building block for constructing two-dimensional (2D) materials. Scientists have successfully synthesized ultrathin films of this compound using solution-processing techniques. These films exhibit remarkable mechanical flexibility and electrical conductivity, making them ideal candidates for flexible electronics. A recent breakthrough reported in *Science* revealed that Quinoxalino[2,3-b]quinoxaline-based films can be integrated into wearable devices, offering unprecedented performance in real-time health monitoring.
In addition to its electronic applications, Quinoxalino[2,3-b]quinoxaline has shown potential in the field of biomedicine. Its large conjugated system allows for strong fluorescence emission under specific conditions, enabling its use as a fluorescent probe for detecting biomolecules. A research team from Stanford University developed a biosensor based on Quinoxalino[2,3-b]quinoxaline that can selectively detect glucose levels in biological fluids with high sensitivity and specificity. This innovation opens new avenues for point-of-care diagnostics and personalized medicine.
The synthesis of Quinoxalino[2,3-b]quinoxaline has also been a topic of extensive research. Traditional methods involve multi-step reactions with low yields and harsh reaction conditions. However, recent advancements in catalytic chemistry have led to the development of more efficient synthesis routes. For example, researchers at MIT reported a one-pot synthesis method using transition metal catalysts that significantly improves the yield and purity of Quinoxalino[2,3-b]quinoxaline. This breakthrough not only simplifies the production process but also reduces costs, making it more accessible for large-scale applications.
Moreover, the environmental impact of Quinoxalino[2,3-b]quinoxaline has been a growing concern as its applications expand. Studies have shown that this compound exhibits low toxicity towards aquatic organisms under controlled conditions. However, further research is needed to fully understand its long-term effects on ecosystems and human health. Regulatory agencies are actively working with scientists to establish guidelines for safe handling and disposal of Quinoxalino[2,3-b]quinoxaline, ensuring its sustainable use in various industries.
In conclusion, Quinoxalino[2,3-b]quinoxaline (CAS No: 258-14-0) is a versatile compound with immense potential across multiple disciplines. Its unique chemical structure enables applications ranging from advanced electronics to biomedical diagnostics. As research continues to uncover new properties and functionalities of this compound, it is poised to play an increasingly important role in shaping future technologies.
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