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[2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID

Compound with spectra: 3 NMR, and 1 MS (GC)

[2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID
SpectraBase Compound ID LdpwMoeWonh
InChI InChI=1S/C7H4F6O4S/c8-6(9,10)5(7(11,12)13)17-4(16)2(18-5)1-3(14)15/h2H,1H2,(H,14,15)
InChIKey HFRHQTUSQPARJE-UHFFFAOYSA-N
Mol Weight 298.16 g/mol
Molecular Formula C7H4F6O4S
Exact Mass 297.973449 g/mol

View Spectrum of [2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y-40-438-2

View Spectrum of [2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-OXATHIOLAN-4-YL]-ACETIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
  • HFRHQTUSQPARJE-UHFFFAOYSA-N
  • 2-[5-keto-2,2-bis(trifluoromethyl)-1,3-oxathiolan-4-yl]acetic acid
[2,2-BIS-(TRIFLUOROMETHYL)-5-OXO-1,3-PXATHIOLAN-4-YL]-ACETYL-CHLORIDE
4-(2'-Isocyanatoethyl)-2,2-bis(trifluoromethyl)-1,3-oxathiolan-5-one
3-[2',2'-bis(Trifluoromethyl)-5'-oxo-1',3'-oxathiolan-4'-yl]-propionyl Chloride
4-(HYDROXYBENZYL)-2,2-DIMETHYL-1,3-OXATHIOLAN-5-ONE
(rac)-6-[2,2-Bis(trifluoromethyl)-5-oxo-1,3-oxazolidin-4-yl]hexanoyl chloride
(rac)-4-[2,2-Bis(trifluoromethyl)-5-oxo-1,3-oxazolidin-4-yl]butanoyl fluoride
4-BENZYL-2,2,4-TRIMETHYL-1,3-OXATHIOLAN-5-ONE
Dimethyl 2,3-bis(benzoylthio)succinate
[bis(trifluoromethyl)methyl] N-[(pentafluoroethylcarbonyl]-2-amino-4-methylpentanoate
[bis(trifluoromethyl)methyl] N-[(pentafluoroethylcarbonyl]-2-amino-4-methylthiobutanoate
Title Journal or Book Year
Synthesis of heteroaryl substituted α-mercapto acids from thiomalic acid using hexafluoroacetone as protecting and activating reagent Journal of Heterocyclic Chemistry 2003
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