• 1. An intensified π-hole in beryllium-doped boron nitride meshes: its determinant role in CO2 conversion into hydrocarbon fuels?
  Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
• 2. An artificial photosynthetic system for photoaccumulation of two electrons on a fused dipyridophenazine (dppz)–pyridoquinolinone ligand?
  Philipp Traber,Stephan Kupfer,Stefanie Gr?fe,Isabelle Baussanne,Martine Demeunynck,Jean-Marie Mouesca,Serge Gambarelli,Vincent Artero,Murielle Chavarot-Kerlidou Chem. Sci., 2018,9, 4152-4159
• 3. An alternative biorefinery approach to address microalgal seasonality: blending with spent coffee grounds
  Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
• 4. An approach to C–N activation: coupling of arenesulfonyl hydrazides and arenesulfonyl chlorides with tert-amines via a metal-, oxidant- and halogen-free anodic oxidation??
  M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
• 5. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782

Benzenamine, 3-chloro-5-(methylsulfonyl)- (CAS No. 62605-99-6)

Benzenamine, 3-chloro-5-(methylsulfonyl)-, also known by its CAS registry number 62605-99-6, is a compound of significant interest in the fields of organic chemistry and materials science. This compound is characterized by its unique structure, which includes a benzene ring substituted with a chlorine atom at the 3-position and a methylsulfonyl group at the 5-position. The presence of these substituents imparts distinct chemical and physical properties to the molecule, making it a valuable compound for various applications.

The molecular formula of Benzenamine, 3-chloro-5-(methylsulfonyl)- is C8H8ClNO3S, and its molecular weight is approximately 217.67 g/mol. The compound exists as a crystalline solid under standard conditions, with a melting point of around 180°C. Its solubility in common solvents such as water and ethanol is moderate, which makes it suitable for various synthetic and analytical procedures.

Recent studies have highlighted the potential of Benzenamine, 3-chloro-5-(methylsulfonyl)- in the development of advanced materials. Researchers have explored its use as a precursor for synthesizing functional polymers and hybrid materials. For instance, the methylsulfonyl group in the molecule has been shown to enhance the thermal stability and mechanical properties of polymer composites when incorporated into their structures.

In addition to its role in materials science, Benzenamine, 3-chloro-5-(methylsulfonyl)- has also been investigated for its potential in pharmaceutical applications. The compound's structure allows for selective binding to certain biological targets, making it a promising candidate for drug design. Recent research has focused on its ability to modulate enzyme activity and its potential as an inhibitor for specific protein kinases.

The synthesis of Benzenamine, 3-chloro-5-(methylsulfonyl)- typically involves multi-step organic reactions. A common approach includes the chlorination of aniline derivatives followed by sulfonation at specific positions on the aromatic ring. The reaction conditions are carefully optimized to ensure high yields and purity of the final product.

From an environmental standpoint, studies have been conducted to assess the biodegradability and toxicity of Benzenamine, 3-chloro-5-(methylsulfonyl)-. Initial findings suggest that the compound exhibits moderate biodegradability under aerobic conditions, though further research is needed to fully understand its environmental impact.

In conclusion, Benzenamine, 3-chloro-5-(methylsulfonyl)- (CAS No. 62605-99-6) is a versatile compound with promising applications in both materials science and pharmaceutical research. Its unique structure and functional groups make it an attractive candidate for developing advanced materials and bioactive molecules. As research continues to uncover new insights into its properties and potential uses, this compound is likely to play an increasingly important role in various scientific disciplines.

• 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)