(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol CAS: 127852-28-2
Catalog Number | XD93681 |
Product Name | (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol |
CAS | 127852-28-2 |
Molecular Formula | |
Molecular Weight | |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is a chiral compound that finds application in various areas, including organic synthesis, pharmaceutical research, and material science.One significant application of (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is its use as a chiral building block in the synthesis of pharmaceutical compounds. Chirality, or the presence of a non-superimposable mirror image, is of utmost importance in drug development. Many biological processes are highly chiral and often interact differently with enantiomers, the two mirror-image forms of a chiral compound. (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol acts as a chiral precursor, enabling the synthesis of a diverse range of pharmaceutical compounds with specific enantiomeric properties. These compounds can exhibit different pharmacological activities, biodistribution, and metabolic profiles. The chiral nature of (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol makes it particularly valuable in the development of safer and more effective drugs.Additionally, (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol has applications in asymmetric catalysis. Asymmetric catalysis plays a crucial role in organic synthesis by enabling the efficient production of enantiopure compounds. The chiral properties of (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol make it an effective ligand and catalyst precursor, facilitating asymmetric transformations in various chemical reactions. This allows chemists to access enantioenriched compounds with high levels of selectivity and efficiency, reducing waste and increasing the overall synthetic yield.Furthermore, (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is used in material science research. Its unique chemical structure and chirality make it a valuable component in the synthesis of specialty materials, such as liquid crystals, polymers, and dendrimers. These materials often possess unique optical, electronic, or mechanical properties, making them useful in applications ranging from display technologies to sensors and advanced materials.In summary, (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is a versatile compound with broad applications in organic synthesis, pharmaceutical research, and material science. Its chiral nature allows for the synthesis of enantiopure compounds, enabling the development of safer and more effective drugs. Additionally, it serves as a valuable catalyst precursor in asymmetric catalysis, facilitating the production of enantioenriched compounds. Finally, (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is utilized in material science research, contributing to the development of specialty materials with unique properties.