65530-60-1 | 3,3,3-Trifluoro-1-propanol

CAS:65530-60-1 | 3,3,3-Trifluoro-1-propanol ,Description

3,3,3-Trifluoro-1-propanol is a fluorinated alcohol compound that has gained significant attention in scientific research. This compound has unique properties that make it a valuable tool for various applications in the field of chemistry, biochemistry, and medicine. In 
 

Scientific Research Applications

Electrophilic Hypervalent Trifluoromethylthio-Iodine(III) Reagent

3,3,3-Trifluoro-1-propanol has been utilized in the design and synthesis of a hypervalent trifluoromethylthio-iodine(III) reagent. This compound has been found to be a versatile electrophilic reagent for transferring a trifluoromethylthio group (-SCF3), demonstrating its utility in chemical synthesis (Yang, Zheng, & Zhang, 2020).

Oxidation of Secondary Alcohols

Research on the kinetics of oxidation of various alcohols, including 3,3,3-Trifluoro-1-propanol, by potassium tetraoxoferrate(VI) has been conducted. This study provides insights into the chemical behavior and reactivity of trifluoro-1-propanol under oxidative conditions (Norcross, Lewis, Gai, Noureldin, & Lee, 1997).

Radical Addition to Trifluoroethylene

In a study focusing on the photochemically initiated addition of 2-propanol to trifluoroethylene, 3,3,3-Trifluoro-1-propanol was explored as a product in the formation of various fluoroalcohols. This research aids in understanding the reactivity of trifluoro-1-propanol in radical addition reactions (Fikar, Trška, Pech, & Liška, 1996).

Photodissociation Dynamics

The photodissociation dynamics of compounds similar to 3,3,3-Trifluoro-1-propanol, such as 3-bromo-1,1,1-trifluoro-2-propanol, have been investigated. This research contributes to the broader understanding of the photophysical and photochemical behaviors of trifluoroalcohols (Indulkar et al., 2011).

Electroreductive Coupling

A study on the electroreductive intermolecular coupling of halofluoro compounds, including trifluoro-1-propanol derivatives, highlights the potential of 3,3,3-Trifluoro-1-propanol in synthetic chemistry, particularly in electrosynthesis applications (Shono, Kise, & Oka, 1991).

Chemical Fixation of CO2 and Epoxides

Research involving 3-Bromo-1,1,1-trifluoro-2-propanol, a compound closely related to 3,3,3-Trifluoro-1-propanol, shows its application in the chemical fixation of CO2 with epoxides. This illustrates the potential role of trifluoro-1-propanol in green chemistry and carbon capture technologies (Ma et al., 2020).

Hydrogen Bonding Studies

Studies on the hydrogen bonding in fluorinated alcohols, including 3,3,3-Trifluoro-1-propanol, provide valuable insights into the molecular interactions and properties of these compounds. This research is essential for understanding the behavior of trifluoro-1-propanol in various chemical environments (Schaal, Häber, & Suhm, 2000).

UV Oxidation in Fluidized Bed Reactor

The use of 3,3,3-Trifluoro-1-propanol has been investigated in the context of UV oxidation in a novel three-phase fluidized bed reactor. This research demonstrates the compound's potential in advanced oxidation processes, particularly in environmental applications such as wastewater treatment (Shih, Tsai, & Huang, 2013).

Conformational Analysis

Conformational analysis of compounds structurally similar to 3,3,3-Trifluoro-1-propanol, like 3,3,3-trifluoro-2-(trifluoromethyl)propanoic acid, provides insights into the structural and electronic properties of trifluoroalcohols. Understanding these properties is crucialfor their application in various scientific fields (Thomas et al., 2016).

Vapor−Liquid Equilibria Studies

Investigations into the vapor−liquid equilibria of systems involving 1-propanol and trifluoromethanesulfonate, closely related to 3,3,3-Trifluoro-1-propanol, reveal important physicochemical data. This information is essential for understanding the thermodynamic behavior of trifluoroalcohols in various solvent systems (Orchillés, Miguel, Vercher, & Martínez-Andreu, 2008) .

Electronic Structure Analysis

The study of the electronic structure of compounds like 3,3,3-trifluoropropene, closely related to 3,3,3-Trifluoro-1-propanol, provides valuable insights into the electronic properties and chemisorption behavior of trifluoroalcohols. Such studies are crucial in materials science and surface chemistry (Grant, Hale, & Stair, 1986).

More Information