2,2,2-Trifluoroethanol CAS: 1493-13-6
Catalog Number | XD93574 |
Product Name | 2,2,2-Trifluoroethanol |
CAS | 1493-13-6 |
Molecular Formula | C2F3KO2 |
Molecular Weight | 152.11 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2,2,2-Trifluoroethanol is a fluorinated alcohol that finds several important applications in various fields, including pharmaceuticals, agrochemicals, and materials science. Its unique chemical properties make it a valuable building block and reagent in synthesis.One major use of 2,2,2-trifluoroethanol is as a solvent and co-solvent. It has the ability to dissolve a wide range of organic and inorganic compounds due to its strong polarity and hydrogen bond donating capacity. This makes it particularly useful in processes that require solubilizing challenging substrates, such as polar and nonpolar solutes, metal salts, or polymers. It is commonly employed in pharmaceutical research and development as a solvent for peptide synthesis and as a co-solvent to enhance the solubility of poorly soluble drugs.2,2,2-Trifluoroethanol is also utilized as a versatile reagent for various chemical transformations. It can undergo nucleophilic substitution, acylation, and condensation reactions due to the presence of both a strong electron-withdrawing trifluoromethyl group and a hydroxy functional group. These reactions can be triggered by the presence of strong bases or acids. It is particularly valuable for reactions that require the introduction or modification of trifluoromethyl substituents, as it serves as a source of the trifluoromethyl group.In organic synthesis, 2,2,2-trifluoroethanol is often utilized for the synthesis of fluorinated compounds. It can act as a precursor to create trifluoromethylated or fluorinated building blocks, which are significant in the development of pharmaceuticals and agrochemicals. The trifluoromethyl group can enhance the bioactivity and metabolic stability of drug molecules, making them attractive targets for medicinal chemistry.Furthermore, 2,2,2-trifluoroethanol is employed as a chiral resolving agent due to its ability to form stable hydrogen bonding complexes with chiral compounds. This property allows for the separation of enantiomers, which are mirror image isomers of a molecule, and is crucial in the production of optically pure pharmaceutical ingredients.While 2,2,2-trifluoroethanol offers numerous advantages in various applications, it is important to handle it with care due to its toxic and potentially hazardous nature. Proper safety measures, including the use of personal protective equipment and working in a well-ventilated area, should be followed to ensure the safety of the user and prevent any accidental exposure.In summary, 2,2,2-trifluoroethanol is a versatile compound that finds multiple uses in different industries. Its ability to act as a solvent, reagent, and chiral resolving agent makes it valuable for various applications, including drug development and materials synthesis. However, caution should be exercised when using it, adhering to proper safety protocols to ensure the well-being of the user and the success of the desired chemical processes.