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ETHYLTHIOPHENYLCETONE
SpectraBase Compound ID 9IIcsevX477
InChI InChI=1S/C9H10OS/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChIKey XZJPOQGUMFRLEW-UHFFFAOYSA-N
Mol Weight 166.24 g/mol
Molecular Formula C9H10OS
Exact Mass 166.045236 g/mol
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum NP-17-4401-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O7-0-771-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-3-2624-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QE-28-SM43-1t (DOI: 10.1002/chem.202202212)
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-3347-7
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-50-297-8
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-7112-0-0
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • ETHYLTHIOBENZOATE
  • THIOBENZOIC_ACIDETHYLESTER
  • ETHYL-THIOLOBENZOATE
  • S-ETHYLTHIOBENZOAT
  • S-ETHYL_THIOBENZOATE
  • Benzenecarbothioic acid, S-ethyl ester
  • S-ethyl benzothioate
Title Journal or Book Year
Flash vacuum pyrolysis of stabilised phosphorus ylides. Part 13.1 Extrusion of Ph3P from sulfinyl ylides and reactivity of the resulting sulfinyl carbenes Journal of the Chemical Society, Perkin Transactions 1 1998
17O NMR Spectra of Carbonyl Compounds ArCOX: Influence of Groups X on the Polarity of the Carbonyl Group Magnetic Resonance in Chemistry 1997
NMR of terminal oxygen. Part 7.17O NMR spectra of benzoyl derivatives of Ge, Se, Te and I: π-bond order and excitation energy in benzoyl compounds J. Chem. Soc., Perkin Trans. 2 1991
17O-NMR-Spektroskopie von Benzoylverbindungen YC6H4 COX: Empfindlichkeit auf Substituenteneinflüsse als Maß für den Elektronenmangel an der Carbonylgruppe Angewandte Chemie 1990
17O and31P NMR of aroylphosphanes, aroylsilanes and aroylphosphonates: Absence of resonance in —COPR2 groups (NMR of terminal oxygen, part 5) Magnetic Resonance in Chemistry 1990
A carbon-13 nuclear magnetic resonance study of thiol esters The Journal of Organic Chemistry 1977

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