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211346

Sigma-Aldrich

(S)-(+)-1-(9-Anthryl)-2,2,2-trifluoroethanol

≥98%

Synonym(s):

(S)-(+)-α-(Trifluoromethyl)anthracene-9-methanol, (S)-(+)-2,2,2-Trifluoro-1-(9-anthryl)ethanol

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About This Item

Empirical Formula (Hill Notation):
C16H11F3O
CAS Number:
Molecular Weight:
276.25
Beilstein/REAXYS Number:
4695162
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

assay

≥98%

optical activity

[α]25/D +29°, c = 6.3 in chloroform

mp

132-135 °C (lit.)

SMILES string

O[C@@H](c1c2ccccc2cc3ccccc13)C(F)(F)F

InChI

1S/C16H11F3O/c17-16(18,19)15(20)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9,15,20H/t15-/m0/s1

InChI key

ICZHJFWIOPYQCA-HNNXBMFYSA-N

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General description

(S)-(+)-1-(9-Anthryl)-2,2,2-trifluoroethanol is a chiral solvating agent (CSA).[1]

Application

(S)-(+)-1-(9-Anthryl)-2,2,2-trifluoroethanol has been used for the NMR spectral determination of optical purity (and in some cases, absolute configuration) of a wide variety of sulfoxides,[2] lactones,[3][4] amines,[5] sulfinate esters,[6] oxaziridines[7] and allenes.[8]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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A Simple 13C NMR Method for the Discrimination of Complex Mixtures of Stereoisomers: All Eight Stereoisomers of a-Tocopherol Resolved.
Lankhorst PP, et al.
Chirality, 27(11), 850-855 (2015)
Journal of Chromatography A, 123, 400-400 (1976)
M J Zhao et al.
Journal of chromatography. B, Biomedical applications, 656(2), 441-446 (1994-06-17)
A relatively rapid, inexpensive, sensitive and stereospecific gas chromatographic-mass spectrometric method was developed for the quantification of S(+) and R(-)-ibuprofen in human plasma. This method uses a commercially available internal standard and has no interference from endogenous substances nor metabolites.
The Journal of Organic Chemistry, 42, 3697-3697 (1977)
Journal of the American Chemical Society, 98, 1832-1832 (1976)

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