• 1. 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
• 2. 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
• 3. An antimonate pyrochlore (H1.23Sr0.45SbO3.48) for photocatalytic oxidation of benzene: effective oxygen usage and excellent activity?
  Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
• 4. An anti-leakage liquid metal thermal interface material
  Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
• 5. An aptasensor for the detection of ampicillin in milk using a personal glucose meter
  Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzene and substituted derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives

Distannathiane, 1,1,1,3,3,3-hexaphenyl-: A Comprehensive Overview

The compound Distannathiane, 1,1,1,3,3,3-hexaphenyl-, also known by its CAS registry number 77-80-5, is a unique organotin compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound belongs to the class of stannanes (organotin compounds), which are characterized by their tin atom bonded to carbon groups. The structure of 1,1,1,3,3,3-hexaphenyl-distannathiane is particularly interesting due to its symmetric and highly substituted nature, making it a valuable subject for both fundamental research and potential applications in various industries.

Firstly, the organotin chemistry of Distannathiane, 1,1,1,3,3,3-hexaphenyl- is notable for its stability and resistance to hydrolysis. This property makes it a promising candidate for use in applications where long-term stability is required, such as in electronic devices or as a component in polymer additives. Recent studies have explored the potential of this compound in polymer stabilization, where its ability to act as a stabilizing agent for polymers has shown remarkable results.

One of the most exciting developments involving 1,1,1,3,3,3-hexaphenyl-distannathiane is its application in nanotechnology. The compound's highly substituted structure provides excellent steric protection to the tin center, which can be exploited in the synthesis of nanoparticles. Research has demonstrated that this compound can serve as a precursor for the formation of tin-based nanoparticles, which have applications in imaging, sensing, and catalysis. For instance, tin-based nanoparticles are being explored for their potential in biomedical imaging due to their biocompatibility and ability to enhance contrast in imaging techniques.

Another area where Distannathiane, 1,1,1,3,3,3-hexaphenyl- has shown promise is in catalysis. The compound's structure allows for precise control over the electronic and steric environment around the tin atom, making it a valuable catalyst precursor. Recent advancements have utilized this compound in the synthesis of homogeneous catalysts for various reactions, including cross-coupling and hydrogenation. These catalytic applications are particularly relevant in the pharmaceutical industry, where efficient and selective catalysis is crucial for drug discovery and production.

Furthermore, 1,1,1,3,3,3-hexaphenyl-distannathiane has been studied for its potential as a building block in organic synthesis. Its symmetric structure and stability make it an ideal candidate for use in the construction of complex molecules. Recent research has focused on the use of this compound in the synthesis of pharmaceutical intermediates, highlighting its versatility and utility in drug development.

It is also worth noting the environmental implications of Distannathiane, 1,1,1,3,3,3-hexaphenyl-. While organotin compounds are generally stable, their environmental fate and toxicity must be carefully considered. Research has shown that this compound exhibits low toxicity to aquatic organisms, making it a relatively environmentally friendly choice for industrial applications.

Looking ahead, the future of 1,1,1,3,3,3-hexaphenyl-distannathiane is likely to be shaped by advancements in nanotechnology, catalysis, and pharmaceutical chemistry. As our understanding of this compound's properties continues to grow, so too will its range of applications. The combination of its unique structure with cutting-edge research techniques positions it as a key player in the development of next-generation materials and technologies.

Finally, the study of Distannathiane, 1,1,1,3,3,3-hexaphenyl- underscores the importance of interdisciplinary collaboration in advancing our knowledge of organotin compounds. By bringing together expertise from organic chemistry, materials science, and biomedical engineering, researchers can unlock new possibilities for this compound's use in a variety of 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)