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phosphorothioic acid, O,O-dimethyl O-4-nitro-m-tolyl ester

Compound with spectra: 3 NMR, 2 FTIR, 1 UV-Vis, and 16 MS (GC)

phosphorothioic acid, O,O-dimethyl O-4-nitro-m-tolyl ester
SpectraBase Compound ID JQPNT1QaTLM
InChI InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3
InChIKey ZNOLGFHPUIJIMJ-UHFFFAOYSA-N
Mol Weight 277.23 g/mol
Molecular Formula C9H12NO5PS
Exact Mass 277.017381 g/mol

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MS (GC) Spectrum
Copyright Copyright © 2023-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS

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MS (GC) Spectrum
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #45487
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)

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MS (GC) Spectrum
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Dr. Rolf Kuehnle
Technique GC/MS

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MS (GC) Spectrum
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Dr. Rolf Kuehnle
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2016-2024  John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Cat. #45487
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)

View Spectrum of phosphorothioic acid, O,O-dimethyl O-4-nitro-m-tolyl ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SRH-2022-10747-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-0-123-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum T-66-561-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum TE-1992-1728-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SEP-40-2441-Fenitrothion (DOI: 10.1002/jssc.201601337)

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SEP-44-SM8-Fenitrothion (DOI: 10.1002/jssc.202100183)

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum PG-1982-427-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-0-280-0

View Spectrum of phosphorothioic acid, O,O-dimethyl O-4-nitro-m-tolyl ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SRH-2022-7532-0

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-12-9-Fenitrothion

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1H NMR Spectrum
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample I. Pastorek, Research Institute of Agrochemical Technology, Bratislava, Czechoslovakia
Solvent CCl4

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31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

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31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DIOXANE-D8:D2O=1:50

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FTIR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample I. Pastorek, Research Institute of Agrochemical Technology, Bratislava, Czechoslovakia
Technique CAPILLARY CELL: NEAT

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UV-Vis Spectrum
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol

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Vapor Phase IR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
  • FENITROTHION;O,O-DIEMTHYL-O-(3-METHYL-4-NITROPHENYL)-PHOSPHOROTHIOATE
  • Fenitrothion
  • Phosphorothioic acid, O,O-dimethyl O-(3-methyl-4-nitrophenyl) ester
  • o,o-Dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioate
  • FENITROTHIONE 1
  • FENITROTHIONE 2
  • O,O-dimethyl O-(3-methyl-4-nitrophenyl) thiophosphate
  • O,O-dimethyl O-4-nitro-m-tolyl phosphorothioate
  • Dimethoxy-(3-methyl-4-nitro-phenoxy)sulfanylidene-phosphorane
phosphorothioic acid, O-ethyl O-methyl O-4-nitro-m-tolyl ester
phosphorothioic acid, O,O-diethyl O-4-nitro-m-tolyl ester
Fenthion sulfoxide
METHYL-3-METHYL-4-NITROPHENYL-PHOSPHOROCHLORIDOTHIONATE
2-(3-methyl-4-nitrophenoxy)propanohydrazide
Phosphoric acid, dimethyl 3-methyl-4-(methylsulfinyl)phenyl ester
Diethyl-4-thiocyanoto-m-tolyl ester of phosphoric acid
Benzenamine, N,N-dibutyl-3-methyl-4-nitro-
Phosphoric acid, 3-(1,1-dimethylethyl)-4-hydroxyphenyl dimethyl ester
Phosphorothioic acid, O-[3-(2,2-dichloro-1,1-difluoroethoxy)phenyl]O,O-dimethyl ester
Title Journal or Book Year
Inclusion of the insecticide fenitrothion in dimethylated-β-cyclodextrin: unusual guest disorder in the solid state and efficient retardation of the hydrolysis rate of the complexed guest in alkaline solution Beilstein Journal of Organic Chemistry 2013

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