53531-34-3
53531-34-3
Chemical Structure
(R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol
- CAS. Nr.: 53531-34-3
- Formula:C16H11F3O
- Molecular Weight:276.25
IUPAC Name: (R)-1-(anthracen-9-yl)-2,2,2-trifluoroethan-1-ol
InChIKey: ICZHJFWIOPYQCA-OAHLLOKOSA-N
SMILES: FC(F)(F)[C@@H](C1=C(C=CC=C2)C2=CC3=C1C=CC=C3)O
Biological Activity: (R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol is utilized as a chiral shift reagent for determining enantiomeric ratios. Additionally, (R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol can be employed for nuclear magnetic resonance (NMR) optical purity determination[1][2].
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(R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol | (R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol is utilized as a chiral shift reagent for determining enantiomeric ratios. Additionally, (R)-(-)-1-(9-Anthryl)-2,2,2-trifluoroethanol can be employed for nuclear magnetic resonance (NMR) optical purity determination. | |||||||||||||||||||||
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References
- [1]. Patti A, et al. Enantioselective Synthesis of (−)-and (+)-Conduritol F via Enzymatic Asymmetrization of cis-Cyclohexa-3, 5-diene-1, 2-diol[J]. The Journal of Organic Chemistry, 1996, 61(18): 6458-6461. [Content Brief]
- [2]. Castañar L, et al. Enantiodifferentiation through frequency‐selective pure‐shift 1H Nuclear magnetic resonance spectroscopy[J]. ChemPhysChem, 2014, 15(5): 854-857. [Content Brief]
