• 1. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 2. Exceptional activity of sub-nm Pt clusters on CdS for photocatalytic hydrogen production: a combined experimental and first-principles study?
  Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
• 3. Evolutionary de novo design of phenothiazine derivatives for dye-sensitized solar cells?
  Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
• 4. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
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• 5. Excellent peroxidase mimicking property of CuO/Pt nanocomposites and their application as an ascorbic acid sensor?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenanthrenes and derivatives Phenanthrenes and derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenanthrenes and derivatives

Professional Introduction to 3-Bromoperylene (CAS No: 23683-68-3)

3-Bromoperylene, with the chemical formula C₂₀HBr₁₂, is a brominated derivative of perylene, a polycyclic aromatic hydrocarbon (PAH) that has garnered significant attention in the field of materials science and pharmaceutical chemistry due to its unique structural and electronic properties. This compound, identified by its CAS number 23683-68-3, is particularly valued for its applications in organic electronics, photodynamic therapy, and as a building block for more complex molecular architectures.

The structure of 3-Bromoperylene consists of a perylene core substituted with a bromine atom at the 3-position. This substitution introduces a reactive site that can be exploited for further functionalization, making it a versatile intermediate in synthetic chemistry. The perylene backbone contributes to its high thermal stability and solubility in organic solvents, which are critical properties for its use in various industrial applications.

In recent years, 3-Bromoperylene has been extensively studied for its potential in the development of advanced materials. Its conjugated system allows for efficient charge transport, making it an attractive candidate for organic semiconductors and light-emitting diodes (OLEDs). Researchers have demonstrated that incorporating 3-Bromoperylene into polymer matrices can enhance the performance of these devices by improving charge mobility and thermal stability.

Moreover, the bromine substituent in 3-Bromoperylene enables cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig couplings, which are pivotal in constructing complex molecular frameworks. These reactions have been leveraged to create novel materials with tailored properties for applications in sensors, catalysts, and drug delivery systems. The ability to modify the perylene core through such reactions underscores the compound's significance as a chemical building block.

One of the most promising areas of research involving 3-Bromoperylene is its application in photodynamic therapy (PDT). Perylene derivatives are known for their strong absorption in the near-infrared (NIR) region, which is ideal for clinical use due to reduced tissue autofluorescence. Studies have shown that 3-Bromoperylene can be used to generate reactive oxygen species upon irradiation with NIR light, leading to targeted destruction of cancer cells. Its high phototoxicity and low toxicity profile make it a compelling candidate for further development as an anticancer agent.

The synthesis of 3-Bromoperylene typically involves bromination of perylene or its derivatives using brominating agents such as N-bromosuccinimide (NBS). This reaction is often carried out under controlled conditions to ensure high selectivity and yield. Advances in synthetic methodologies have enabled the production of 3-Bromoperylene with high purity, which is essential for its application in sensitive areas like pharmaceuticals and biomedicine.

In addition to its material science applications, 3-Bromoperylene has found utility in pharmaceutical research. Its structural motif is shared by several bioactive compounds, suggesting that it may have therapeutic potential. While direct clinical applications are still under investigation, preclinical studies have hinted at its role in modulating biological pathways associated with inflammation and oxidative stress. These findings open up new avenues for exploring 3-Bromoperylene-based drugs targeting various diseases.

The photophysical properties of 3-Bromoperylene have also been thoroughly examined. Its fluorescence characteristics make it suitable for use as a fluorescent probe in biological assays. Researchers have utilized it to study cellular processes such as DNA intercalation and protein interaction. The ability to track these processes non-invasively has significant implications for diagnostic tools and drug discovery platforms.

As research continues to uncover new applications for 3-Bromoperylene, the demand for high-quality sources of this compound is likely to increase. Manufacturers specializing in fine chemicals have responded by optimizing production processes to meet the growing need for purity and consistency. This ensures that researchers and industry professionals can rely on CAS No: 23683-68-3 products for their most demanding applications.

In conclusion, 3-Bromoperylene represents a fascinating compound with diverse applications spanning from advanced materials to pharmaceuticals and biomedicine. Its unique structure, reactivity, and functional properties make it indispensable in modern chemical research. As scientists continue to explore its potential, we can expect even more innovative uses to emerge, further solidifying its role as a cornerstone molecule in the chemical industry.

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