• 1. Novel triazine derivatives with deep LUMO energy levels as the electron-accepting components of exciplexes
  Jing Guo,Cai-Jun Zheng,Ke Ke,Ming Zhang,Hao-Yu Yang,Jue-Wen Zhao,Ze-Yu He,Hui Lin,Si-Lu Tao,Xiao-Hong Zhang J. Mater. Chem. C 2021 9 939
• 2. Combination of gold and iridium catalysts for the synthesis of N-alkylated amides from nitriles and alcohols
  Feng Li,Juan Ma,Lei Lu,Xiaofeng Bao,Wanying Tang Catal. Sci. Technol. 2015 5 1953
• 3. Rhodium(iii)-catalyzed C4-amidation of indole-oximes with dioxazolones via C–H activation
  Shi-Biao Tang,Xiao-Pan Fu,Gao-Rong Wu,Li-Li Zhang,Ke-Zuan Deng,Jin-Yue Yang,Cheng-Cai Xia,Ya-Fei Ji Org. Biomol. Chem. 2020 18 7922
• 4. Effect of a novel compound as dietary supplement on growth of decapod crustaceans
  Sajal Shrivastava,S. Adline Princy RSC Adv. 2015 5 65546
• 5. Direct oxidative amidation of aldehydes with amines catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions via a dual-catalysis process
  Renzhong Fu,Yang Yang,Jin Zhang,Jintao Shao,Xuming Xia,Yunsheng Ma,Rongxin Yuan Org. Biomol. Chem. 2016 14 1784

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Halobenzoic acids and derivatives
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

M-Bromobenzamide (CAS No. 22726-00-7): A Comprehensive Overview in Modern Chemical Research

M-Bromobenzamide, chemically identified by the CAS number 22726-00-7, is a significant compound in the realm of chemical and pharmaceutical research. This aromatic amide derivative has garnered considerable attention due to its versatile applications and structural properties, making it a valuable tool in various synthetic and biological studies.

The molecular structure of M-Bromobenzamide consists of a benzene ring substituted with a bromine atom at the meta position and an amide functional group. This unique configuration imparts distinct reactivity and functionality, enabling its use in multiple chemical transformations. The presence of the bromine atom enhances its utility as a electrophilic aromatic substitution precursor, while the amide group facilitates further derivatization, making it a cornerstone in medicinal chemistry.

In recent years, M-Bromobenzamide has been extensively studied for its potential in drug development. Its role as an intermediate in synthesizing more complex molecules has been well-documented. Researchers have leveraged its reactivity to develop novel therapeutic agents targeting various diseases. For instance, studies have shown its efficacy in the synthesis of kinase inhibitors, which are crucial in treating cancers and inflammatory disorders.

One of the most compelling aspects of M-Bromobenzamide is its application in the field of organic synthesis. The compound serves as a key building block for constructing more intricate molecular frameworks. Its ability to undergo selective reactions under controlled conditions makes it an indispensable reagent in laboratory settings. The development of new synthetic methodologies has further highlighted its importance, with recent advancements focusing on improving yield and purity.

The pharmaceutical industry has also embraced M-Bromobenzamide for its potential in developing new drugs. Its structural features allow for modifications that can enhance drug bioavailability and target specificity. For example, researchers have explored its use in creating protease inhibitors, which are vital in treating viral infections such as HIV and hepatitis C. The compound's ability to interact with biological targets at a molecular level has opened new avenues for therapeutic intervention.

Furthermore, M-Bromobenzamide has found applications beyond pharmaceuticals. In materials science, it has been utilized to develop novel polymers and coatings with enhanced thermal and chemical stability. Its incorporation into these materials improves their performance under harsh conditions, making them suitable for industrial applications.

The environmental impact of using M-Bromobenzamide has also been a subject of interest. Efforts have been made to optimize synthetic routes to minimize waste and reduce environmental footprint. Green chemistry principles have guided these initiatives, ensuring that the production process aligns with sustainable practices.

Future research directions for M-Bromobenzamide are promising and multifaceted. Ongoing studies aim to uncover new synthetic pathways that could make its production more efficient and cost-effective. Additionally, exploring its potential in drug discovery continues to be a priority, with researchers focusing on identifying novel therapeutic applications.

In conclusion, M-Bromobenzamide (CAS No. 22726-00-7) is a versatile compound with significant implications across various scientific disciplines. Its unique structural properties and reactivity make it an invaluable tool in chemical synthesis and pharmaceutical development. As research progresses, the applications of M-Bromobenzamide are expected to expand, contributing to advancements in medicine, materials science, and beyond.

• 698-67-9(4-Bromobenzamide)
• 170229-98-8(4-Bromo-3-methylbenzamide)
• 49834-22-2(N-Methyl 3-bromobenzamide)
• 864825-81-0(4-Bromo-3,5-dimethylbenzamide)
• 183723-09-3(3-Bromo-4-methylbenzamide)
• 854633-21-9(5-Bromo-2-methylbenzamide)
• 490038-15-8(4-Bromophthalamide)
• 175205-85-3(3,5-Dibromobenzamide)
• 1007578-82-6(3-Bromo-5-methylbenzamide)
• 868776-08-3(4-Bromo-2-methyl-benzamide)