• 1. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
• 2. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 3. Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
  Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
• 4. Fe3O4 nanosphere@microporous organic networks: enhanced anode performances in lithium ion batteries through carbonization?
  Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
• 5. Emulsion soft templating of carbide-derived carbon nanospheres with controllable porosity for capacitive electrochemical energy storage?
  M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives Brominated biphenyls

4-(2-Bromophenyl)phenol: A Comprehensive Overview

4-(2-Bromophenyl)phenol, also known by its CAS registry number CAS No. 70066-66-9, is a chemical compound that has garnered significant attention in various fields of scientific research. This compound is a derivative of phenol, with a bromine atom substituted at the 2-position of the phenyl ring. The structure of 4-(2-Bromophenyl)phenol consists of two aromatic rings connected by a single bond, with the bromine atom located on the second ring and the hydroxyl group (-OH) on the fourth position of the first ring.

The synthesis of 4-(2-Bromophenyl)phenol typically involves nucleophilic aromatic substitution or coupling reactions, depending on the desired regioselectivity and yield. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste. These methods often utilize transition metal catalysts, such as palladium or copper complexes, to facilitate coupling reactions between aryl halides and phenolic compounds.

4-(2-Bromophenyl)phenol has been extensively studied for its potential applications in materials science, particularly in the development of advanced materials such as organic semiconductors and stimuli-responsive polymers. The compound's unique electronic properties, derived from its aromatic structure and substituents, make it an ideal candidate for use in organic electronics. For instance, researchers have explored its role in creating high-performance organic field-effect transistors (OFETs), where it serves as a key component in the active layer due to its excellent charge transport properties.

In addition to its electronic applications, 4-(2-Bromophenyl)phenol has also been investigated for its biological activity. Recent studies have demonstrated that this compound exhibits potent anti-inflammatory and antioxidant properties, making it a promising candidate for drug development. Its ability to modulate cellular signaling pathways involved in inflammation suggests potential therapeutic applications in conditions such as arthritis and neurodegenerative diseases.

The environmental impact of 4-(2-Bromophenyl)phenol is another area of active research. Given its widespread use in industrial and pharmaceutical applications, understanding its fate and toxicity in aquatic environments is crucial. Recent eco-toxicological studies have shown that while the compound exhibits moderate toxicity to aquatic organisms, its persistence in the environment is relatively low due to rapid biodegradation under aerobic conditions.

In conclusion, 4-(2-Bromophenyl)phenol, with its CAS number CAS No. 70066-66-9, is a versatile compound with diverse applications across multiple scientific disciplines. From materials science to pharmacology, ongoing research continues to uncover new potentials for this compound, solidifying its importance in both academic and industrial settings.

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