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34143-74-3 | 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluoro-1-decanethiol

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3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluoro-1-decanethiol (HDFD) is a synthetic organosulfur compound that has been studied for its potential applications in biochemistry and medicine. It is a type of thiol, a sulfur-containing molecule with a distinctive odor. HDFD has been shown to possess a number of bioche...

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CAS:34143-74-3 | 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluoro-1-decanethiol ,Description

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluoro-1-decanethiol (HDFD) is a synthetic organosulfur compound that has been studied for its potential applications in biochemistry and medicine. It is a type of thiol, a sulfur-containing molecule with a distinctive odor. HDFD has been shown to possess a number of biochemical and physiological effects, which makes it a promising candidate for further research and development.
 

Scientific Research Applications

 

  • Electrode Work Function Modulation: This compound, as part of self-assembled monolayers (SAMs), can modulate the work function of silver, useful in fabricating devices like organic light-emitting diodes (OLEDs) (Wu, Yu, & Tao, 2009).
  • Monitoring Self-Assembly Process: It assists in studying the self-assembly process of decanethiol on gold surfaces, providing insights into surface chemistry and material science (R. Y. and Uosaki, 1997).
  • Long-Range Electron Tunneling: This compound is relevant in studying long-range intervalence electron tunneling, offering potential applications in the development of electronic materials (Stein, Lewis, & Seitz, 1982).
  • Synthesis of Fluorosilicone: Its use in the synthesis of fluorosilicone with highly fluorinated alkyl side chains indicates its importance in creating specialized polymers (Furukawa & Kotera, 2002).
  • Development of Hydrophobic Coatings: It contributes to the synthesis of water-based non-stick hydrophobic coatings, a significant application in material science and engineering (Schmidt et al., 1994).
  • Microfocus Ion and Electron Beam Bombardment: This compound is used in patterning self-assembled alkanethiol monolayers on silver, which is crucial for semiconductor or biosensor device fabrication (Gillen et al., 1994) .
  • Electron Transport in Monolayer Films: It's involved in the study of electron transport through alkanethiolate films, which is essential for understanding electrical properties at the molecular level (Stolarczyk & Bilewicz, 2006).
  • Synthesis of Colorless Polyimides: The compound plays a role in synthesizing polyimides characterized by colorlessness and high solubility, useful in materials science (Yang & Su, 2005).
  • Borane-Dimethyl Sulfide Reactions: It's a component in the synthesis of borane-dimethyl sulfide, a recyclable and hydroborating agent (Patel, 2009) .

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