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  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives Brominated biphenyls

3-Bromo-5-(2-methylphenyl)phenol: A Comprehensive Overview

3-Bromo-5-(2-methylphenyl)phenol, also known by its CAS number 1261888-69-0, is an organic compound with a unique structure that has garnered attention in various fields of chemistry and materials science. This compound belongs to the class of phenolic compounds, which are known for their versatile applications in both industrial and biomedical settings. The molecule consists of a phenol ring substituted with a bromine atom at the 3-position and a 2-methylphenyl group at the 5-position, making it a derivative of phenol with specific functional groups that contribute to its reactivity and properties.

The synthesis of 3-Bromo-5-(2-methylphenyl)phenol typically involves multi-step organic reactions, often starting from readily available aromatic compounds. The bromination step is a critical part of the synthesis, where a bromine atom is introduced at the desired position on the phenol ring. This process often requires precise control over reaction conditions, including temperature and catalysts, to ensure high yields and selectivity. The substitution pattern of this compound makes it an interesting candidate for further functionalization, enabling its use as an intermediate in the synthesis of more complex molecules.

Recent studies have highlighted the potential applications of 3-Bromo-5-(2-methylphenyl)phenol in drug discovery and development. Its unique structure allows for interactions with various biological targets, making it a promising candidate for designing bioactive molecules. For instance, researchers have explored its role as an anti-inflammatory agent due to its ability to modulate key enzymes involved in inflammatory pathways. Additionally, its antioxidant properties have been investigated in the context of neurodegenerative diseases, where oxidative stress plays a significant role.

In materials science, 3-Bromo-5-(2-methylphenyl)phenol has been studied as a precursor for advanced materials such as polymers and nanoparticles. Its phenolic hydroxyl group can participate in hydrogen bonding, which is crucial for forming stable polymer networks. Moreover, the bromine substituent introduces electron-withdrawing effects, enhancing the material's stability under harsh conditions. These properties make it a valuable building block for developing high-performance materials used in electronics and biomedical devices.

The chemical stability of 3-Bromo-5-(2-methylphenyl)phenol is another aspect that has been extensively studied. Under normal storage conditions, the compound exhibits good stability, but exposure to light or oxidizing agents can lead to degradation. Understanding these degradation pathways is essential for optimizing storage conditions and ensuring the compound's reliability in various applications.

In conclusion, 3-Bromo-5-(2-methylphenyl)phenol is a multifaceted compound with significant potential across diverse fields. Its unique structure, synthesis methods, and biological activity make it an intriguing subject for further research. As ongoing studies continue to uncover new applications and insights into its properties, this compound is poised to play an increasingly important role in both academic and industrial settings.

• 21811-40-5(3,4-bis(4-bromophenyl)-2,6-diphenylphenol)
• 1261929-64-9(3-Bromo-5-(3-methylphenyl)phenol)
• 1261929-70-7(3-Bromo-5-(2,5-dimethylphenyl)phenol)
• 1261924-91-7(3-Bromo-5-(2,3-dimethylphenyl)phenol)
• 1261888-71-4(3-Bromo-5-(3-hydroxymethylphenyl)phenol)
• 149950-41-4(4'-BROMO-BIPHENYL-3-OL)
• 934758-97-1(4-BROMO-4'-METHOXY-2'-METHYLBIPHENYL)
• 1261888-74-7(3-Bromo-5-(naphthalen-2-YL)phenol)
• 1261897-54-4(3-Bromo-5-(4-ethoxy-2-methylphenyl)phenol)
• 1261925-01-2(3-Bromo-5-(3,5-dimethylphenyl)phenol)