• 1. Establishing the accuracy of position-specific carbon isotope analysis of propane by GC-pyrolysis-GC-IRMS
  ChangjieLiu,PengLiu,XiaofengWang,XiaoqiangLi,JuskeHorita
• 2. Fast synthesis of copper nanoclusters through the use of hydrogen peroxide additive and their application for the fluorescence detection of Hg2+ in water samples?
  Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
• 3. Dissociative dynamics of O2 on Ag(110)?
  Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
• 4. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147
• 5. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792

6-Quinolinamine,7-chloro- (CAS No. 6312-75-0): A Comprehensive Overview

The compound 6-Quinolinamine,7-chloro-, also identified by its CAS registry number 6312-75-0, is a significant molecule in the field of organic chemistry. This compound belongs to the quinoline family, which is a heterocyclic aromatic system with a nitrogen atom at position 1. The presence of the amino group at position 6 and the chlorine substituent at position 7 introduces unique chemical properties that make this compound a subject of interest in various research domains.

Recent studies have highlighted the potential of 6-Quinolinamine,7-chloro- in drug discovery and material science. Its structural features, including the conjugated aromatic system and the electron-withdrawing chlorine group, make it a versatile building block for synthesizing bioactive molecules. Researchers have explored its role in inhibiting certain enzymes and its potential as a precursor for developing anti-cancer agents.

The synthesis of 6-Quinolinamine,7-chloro- involves multi-step organic reactions, often utilizing chlorination and amination techniques. These methods have been optimized in recent years to improve yield and purity. The compound's stability under various reaction conditions has also been studied extensively, providing insights into its suitability for large-scale production.

In terms of applications, 6-Quinolinamine,7-chloro- has shown promise in the development of advanced materials. Its ability to form coordination complexes with metal ions has led to its use in creating novel catalysts and sensors. Additionally, its photochemical properties have been investigated for potential applications in optoelectronics.

From an environmental perspective, understanding the fate and transport of 6-Quinolinamine,7-chloro- in natural systems is crucial. Recent research has focused on its biodegradation pathways and toxicity profiles to aquatic organisms. These studies aim to ensure that its use does not pose significant risks to ecosystems.

In conclusion, 6-Quinolinamine,7-chloro- (CAS No. 6312-75-0) stands out as a valuable compound with diverse applications across multiple scientific disciplines. Its chemical properties and structural features continue to inspire innovative research directions, making it a key focus for future advancements in organic chemistry and related fields.

• 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)