• 1. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
  Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
• 2. Excellent kinetics of single-phase Gd-doped ceria fuel electrodes in solid oxide cells?
  Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
• 3. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
• 4. Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components?
  Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
• 5. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640

Compound CAS No. 26928-16-5: 2-Propenoic Acid, 3-(4-Chlorophenyl)-2-Fluoro-, (2Z)-

The compound with CAS number 26928-16-5, commonly referred to as 2-Propenoic acid, 3-(4-chlorophenyl)-2-fluoro-, (2Z)-, is a highly specialized organic compound with significant applications in various scientific and industrial domains. This compound is characterized by its unique structure, which includes a propenoic acid backbone substituted with a 4-chlorophenyl group and a fluorine atom at specific positions, resulting in the (Z) configuration.

The synthesis of this compound involves advanced organic chemistry techniques, often requiring precise control over reaction conditions to achieve the desired stereochemistry. Recent studies have highlighted the importance of such compounds in the development of novel materials and pharmaceuticals. For instance, researchers have explored the potential of 3-(4-chlorophenyl)-substituted propenoic acids in creating bioactive molecules with anti-inflammatory and anticancer properties.

In terms of physical properties, CAS No. 26928-16-5 exhibits a melting point of approximately 150°C and a boiling point around 300°C under standard conditions. Its solubility in common solvents such as dichloromethane and ethanol has been well-documented, making it suitable for various laboratory applications. The compound's stability under different environmental conditions has also been a subject of recent investigations, particularly in relation to its potential use in outdoor applications.

The application of this compound extends beyond traditional chemical synthesis. It has found significant use in polymer science, where its ability to form stable copolymers has been leveraged to create high-performance materials for electronic devices. Additionally, its role as an intermediate in the synthesis of more complex molecules has been pivotal in advancing drug discovery efforts.

Recent advancements in computational chemistry have enabled researchers to model the electronic structure of CAS No. 26928-16-5 with unprecedented accuracy. These studies have revealed insights into its reactivity and interaction with other molecules, paving the way for innovative applications in catalysis and green chemistry.

In conclusion, CAS No. 26928-16-5, or 2-Propenoic acid, 3-(4-chlorophenyl)-2-fluoro-, (2Z)-, stands as a testament to the ingenuity of modern chemical synthesis and its vast potential across multiple disciplines. As ongoing research continues to uncover new properties and applications, this compound remains at the forefront of scientific 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)