• 1. An alumina stabilized graphene oxide wrapped SnO2 hollow sphere LIB anode with improved lithium storage?
  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
• 2. An astrophysically-relevant mechanism for amino acid enantiomer enrichment
  Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
• 3. An integrated process of CO2 capture and in situ hydrogenation to formate using a tunable ethoxyl-functionalized amidine and Rh/bisphosphine system?
  Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
• 4. An artificial CO-releasing metalloprotein built by histidine-selective metallation?
  Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
• 5. An atomically efficient, highly stable and redox active Ce0.5Tb0.5Ox (3% mol.)/MgO catalyst for total oxidation of methane?
  Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Nitrobenzenes Nitrophenyl ethers

Introduction to Benzene Methanamine, 5-Methoxy-2-Nitro-

Benzene Methanamine, 5-Methoxy-2-Nitro- (CAS No. 67567-42-4) is a highly specialized organic compound with significant applications in various fields of chemistry and material science. This compound is characterized by its unique molecular structure, which includes a benzene ring substituted with methoxy and nitro groups, along with a methanamine functional group. The combination of these substituents imparts distinctive chemical properties, making it a valuable compound for research and industrial applications.

The benzene ring serves as the central framework of this molecule, providing stability and a platform for the attachment of other functional groups. The methoxy group (-OCH3) at the 5-position introduces electron-donating effects, while the nitro group (-NO2) at the 2-position imparts strong electron-withdrawing characteristics. This balance of electron-donating and withdrawing groups creates a molecule with unique electronic properties, which are highly desirable in various chemical reactions and applications.

Recent studies have highlighted the potential of Benzene Methanamine, 5-Methoxy-2-Nitro- in the field of drug discovery. Its ability to interact with biological systems through specific receptor binding has made it a promising candidate for developing new pharmaceutical agents. Researchers have explored its role in modulating enzyme activity and its potential as an inhibitor or activator in various biochemical pathways.

In addition to its biological applications, this compound has shown remarkable properties in material science. Its ability to form stable complexes with metal ions has led to its use in the synthesis of coordination polymers and metal-organic frameworks (MOFs). These materials have potential applications in gas storage, catalysis, and sensing technologies.

The synthesis of Benzene Methanamine, 5-Methoxy-2-Nitro- involves a series of carefully controlled reactions. The process typically begins with the nitration of an appropriate benzene derivative, followed by methylation and subsequent amine substitution. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste.

From an environmental perspective, understanding the toxicological profile of Benzene Methanamine, 5-Methoxy-2-Nitro- is crucial for ensuring safe handling and disposal practices. Studies have shown that while it exhibits moderate toxicity in acute exposure scenarios, chronic exposure risks remain under investigation. Regulatory bodies are continuously monitoring its use to ensure compliance with safety standards.

In conclusion, Benzene Methanamine, 5-Methoxy-2-Nitro- (CAS No. 67567-42-4) is a versatile compound with wide-ranging applications across multiple disciplines. Its unique chemical structure and functional groups make it an invaluable tool for researchers and industries alike. As ongoing research continues to uncover new insights into its properties and potential uses, this compound is poised to play an even greater role in advancing scientific knowledge and technological innovation.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)