769-39-1 | 2,3,5,6-Tetrafluorophenol

CAS:769-39-1 | 2,3,5,6-Tetrafluorophenol ,Description

2,3,5,6-Tetrafluorophenol (TFP) is a synthetic compound that has a wide range of applications in the scientific research and industrial sectors. It is a white, crystalline solid with a melting point of 39-41°C and a boiling point of 115-117°C. TFP is a highly fluorinated phenol that is used in the synthesis of various compounds, such as pharmaceuticals, pesticides, and dyes. It is also used as an intermediate in the production of specialty chemicals, such as perfluorinated compounds, which are used in a variety of applications. In addition, TFP is used as a reagent in organic synthesis and in the preparation of a variety of organic compounds.
 

Scientific Research Applications

Emission Spectra Studies

The emission spectra of 2,3,5,6-tetrafluorophenol cations in the gaseous phase have been studied, revealing insights into electronic transitions and the properties of these cations. This research provides valuable information for understanding the fundamental characteristics of fluoro-substituted phenols (Maier, Marthaler, Mohraz, & Shiley, 1980).

pH-Sensitive Probes in Liposomal Systems

2,3,5,6-Tetrafluorophenol has been investigated as a pH-sensitive probe in mixed liposomal systems. This research is significant for understanding how these probes interact with different lipid membranes, which is crucial for applications in biochemical and medical research (Gasbarri & Angelini, 2014).

Laser Induced Fluorescence in Matrix

The laser-induced fluorescence spectra of 2,3,5,6-tetrafluorophenol cations in a neon matrix have been obtained, providing detailed insights into the spectral characteristics and electronic states of these molecules (Bondybey, English, Miller, & Shiley, 1983).

Cytochrome P450-Mediated Oxidation

A study on the cytochrome P450-mediated oxidation of 2,3,5,6-tetrafluorophenol shows its conversion to tetrafluorohydroquinone, providing insights into biochemical reactions and potential applications in understanding metabolic pathways (Besten, Bladeren, Duizer, Vervoort, & Rietjens, 1993).

Electron Paramagnetic Resonance Spectroscopy

Research on 2,3,5,6-tetrafluorophenylnitren-4-yl using electron paramagnetic resonance (EPR) spectroscopy has provided new insights into the electronic properties of this radical, which is valuable for understanding high-energy molecular states (Sander, Grote, Kossmann, & Neese, 2008).

Synthesis Methods

An efficient approach to the synthesis of 2,3,4,5-tetrafluorophenol has been developed, which is crucial for producing this compound for various research applications (Tretyakov, Maksimov, Nikul’shin, & Mezhenkova, 2021).

Application in Lithium-Ion Batteries

2,3,5,6-Tetrafluorophenol derivatives have been investigated for use as additives in lithium-ion batteries, contributing to the development of safer and more efficient energy storage technologies (Weng, Zhang, Schlueter, Redfern, Curtiss, & Amine, 2011).

Photostability in Organic Compounds

Research on the stabilization of certain organic compounds against electrocyclization, with 2,3,5,6-tetrafluorophenol as a key component, has implications for the development of photostable materials (Freudenberg, Rominger, & Bunz, 2016).

Precursor for Radiolabeling in PET Imaging

The synthesis of compounds derived from 2,3,5,6-tetrafluorophenol has been explored for use in radiolabeling peptides for PET imaging, a crucial technique in nuclear medicine (Davis & Fettinger, 2018).

Development of Low Surface Energy Materials

Studies on fluorinated styrene-based materials incorporating 2,3,5,6-tetrafluorophenol have been conducted, providing insights into the development of materials with low surface energy, which have wide-ranging applications (Borkar, Jankova, Siesler, & Hvilsted, 2004).

Sterically Encumbered Systems for Phosphorus Centers

Research on tetraarylphenyls, including 2,3,5,6-tetrafluorophenol derivatives, has been conducted to develop compounds with low-coordinate phosphorus centers, which are significant in the field of inorganic chemistry (Shah, Concolino, Rheingold, & Protasiewicz, 2000).

Dechlorination by Anaerobic Microorganisms

The dechlorination of a polychlorinated biphenyl congener by anaerobic microorganisms, involving 2,3,5,6-tetrafluorophenol, has been studied, providing insights into environmental remediation processes (Van Dort & Bedard, 1991).

Fluorescence Emission in Optoelectronic Devices

The optical properties of 2,3,5,6-Tetrafluoro-7,7,8,8-tetracyanoquinodimethane, including fluorescence emission, have been investigated, contributing to the design of energy technology systems (Rubino, Camellini, & Kriegel, 2021).

Porphyrin Synthesis

An efficient synthesis of 2,3,5,6-tetrafluoro-4-iodo-benzaldehyde, a compound derived from 2,3,5,6-tetrafluorophenol, has been developed for use in porphyrin synthesis, which has implications in the field of organic chemistry (Leroy et al., 2004).

Development of Fluorescent Sensors

The construction of new arene-ruthenium rectangles using 2,3,5,6-tetrafluorophenol derivatives and their application in the fluorescent detection of nitroaromatics has been researched, important for developing sensitive chemical sensors (Dubey et al., 2014).

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