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60686-64-8

60686-64-8 | 2,2,2-TRIFLUORO-1-(9-ANTHRYL)ETHANOL

CAS No: 60686-64-8 Catalog No: AG003F6X MDL No:

Product Description

Catalog Number:
AG003F6X
Chemical Name:
2,2,2-TRIFLUORO-1-(9-ANTHRYL)ETHANOL
CAS Number:
60686-64-8
IUPAC Name:
1-anthracen-9-yl-2,2,2-trifluoroethanol
InChI:
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
InChI Key:
ICZHJFWIOPYQCA-UHFFFAOYSA-N

Properties

Complexity:
319  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
276.076g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
276.258g/mol
Monoisotopic Mass:
276.076g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
5  

Literature

Title Journal
A versatile chiral selector for determination of enantiomeric composition of fluorescent and nonfluorescent chiral molecules using steady-state fluorescence spectroscopy. Chirality 20090201
Empirical development of a binary adsorption isotherm based on the single-component isotherms in the framework of a two-site model. Journal of chromatography. A 20070105
The use of poly(sodium N-undecanoyl-L-leucylvalinate), poly(sodium N-undecanoyl-L-leucinate) and poly(sodium N-undecanoyl-L-valinate) surfactants as chiral selectors for determination of enantiomeric composition of samples by multivariate regression modeling of fluorescence spectral data. Journal of fluorescence 20060901
A screening method for chiral selectors that does not require covalent attachment. Journal of the American Chemical Society 20060222
Chromatographic behavior of the enantiomers of 2,2,2-trifluoro-1-(9-anthryl)ethanol on a quinidine-carbamate chiral stationary phase. Journal of chromatography. A 20051014
Adsorption of the enantiomers of 2,2,2-trifluoro-1-(9-anthryl)-ethanol on silica-bonded chiral quinidine-carbamate. Journal of chromatography. A 20041203
Determination of the enantiomeric purity of the phytoalexins spirobrassinins by 1H NMR using chiral solvation. Bioorganic & medicinal chemistry letters 20041115
High-performance liquid chromatographic enantioseparations on capillary columns containing monolithic silica modified with cellulose tris(3,5-dimethylphenylcarbamate). Journal of separation science 20040701
Structural analysis of amylose tris(3,5-dimethylphenylcarbamate) by NMR relevant to its chiral recognition mechanism in HPLC. Journal of the American Chemical Society 20021023
Enantiomeric separations using poly(L-valine) and poly(L-leucine) surfactants. Investigation of steric factors near the chiral center. Journal of chromatography. A 20020809

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