John Wiley & Sons, Inc. SpectraBase; SpectraBase Compound ID=K6Ryd3y0FvR

(accessed ).
Chlorobenzene
SpectraBase Compound ID K6Ryd3y0FvR
InChI InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H
InChIKey MVPPADPHJFYWMZ-UHFFFAOYSA-N
Mol Weight 112.56 g/mol
Molecular Formula C6H5Cl
Exact Mass 112.007978 g/mol
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Source of Sample J. T. Baker Chemical Company
Technique NEAT
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Source of Sample Merck-Schuchardt Hohenbrunn
Technique Cell Spectrometer= Bruker IFS 85
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Source of Sample Riedel de Haen
Technique layer between KBr
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Source of Spectrum SCHOLL
Technique LIQUID, ~10 MICROMETERS
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Source of Sample Hooker Chemical Corporation
Technique NEAT
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Source of Sample Hooker Chemical Corporation
Technique BETWEEN SALTS
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Technique CAPILLARY CELL: NEAT
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Source of Sample Sigma-Aldrich Company LLC
Source of Spectrum Forensic Spectral Research
Catalog Number 8650
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Source of Sample Sigma-Aldrich
Catalog Number 319996
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Source of Sample Hooker Chemical Corporation, New York, New York
Solvent CDCl3; Reference=TMS; Temperature 297K
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Source of Sample HOOKER CHEMICAL CORPORATION, NIAGARA FALLS, NEW YORK
Solvent CCl4
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Source of Sample Fluka Feinchemikalien GmbH Neu-Ulm
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Copyright Copyright © 2018-2020 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2020-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 242829
Copyright Copyright © 1989, 1990-2020 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Prof. Buback, University of Goettingen, Germany
Copyright Copyright © 1989, 1990-2020 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Prof. Buback, University of Goettingen, Germany
Copyright Copyright © 2002-2020 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Database Compilation Copyright © 2020 Wiley-VCH Verlag GmbH & Co. KGaA. Copyright © 2020 DigiLab GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2020
Technique GC/MS
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Source of Spectrum AA-0-370-3
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Source of Spectrum HE-1982-0-0
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Source of Spectrum NW-432-0-0
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Source of Spectrum EP-3658-0-0
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Source of Spectrum JA-3-549-0
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Source of Spectrum EP-3222-0-0
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Source of Spectrum WS-1986-72-0
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Source of Spectrum D5-0-0-0
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Source of Spectrum JZ-1992-623-0
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Source of Spectrum TE-1992-161-0
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Source of Spectrum SB-46-162-0
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Source of Sample Hooker Chemical Corporation, Niagara Falls, New York
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20
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Solvent DIOXANE
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent C3D6O acetone-d6
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3 chloroform-d
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent Dioxane
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Solvent CCl4
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Solvent Neat liquid
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Solvent CHCl3
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Solvent Acetone
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
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Solvent DMSO-D6
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Solvent CDCl3
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Solvent NEAT
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Solvent CYClOHEXANE
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Solvent CDCl3:CCl4
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Solvent ACETONE
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Solvent DMSO
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Solvent Unknown
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Solvent CDCl3;C~1M
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD:CD2Cl2
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Solvent DMSO-D6
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Solvent DMSO-D6
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Source of Sample Sigma-Aldrich Company LLC
Source of Spectrum Forensic Spectral Research
Catalog Number 8650
Copyright Copyright © 2017-2020 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2017-2020 John Wiley & Sons, Inc. All Rights Reserved.
Catalog Number 242829
  • Monochlorobenzene
  • MCB
  • Chlorbenzol
  • Phenyl chloride
  • Benzene chloride
  • Benzene, chloro-
  • Chlorobenzol
  • MVPPADPHJFYWMZ-UHFFFAOYSA-N
Title Journal or Book Year
On the intermediacy of phenyl hydrogen sulfates in the sulfonation of phenols. Sulfonation of phenol, anisole, methyl phenyl sulfate, the 2-halogenophenols, a series of phenyl methanesulfonates together with 2,6-dimethylaniline and its N-methylsulfonyl de Recueil des Travaux Chimiques des Pays-Bas 2010
Nitrogen-15 NMR Studies on Hydrazines. 2— Substituent Effect Analysis inortho-Substituted Phenylhydrazines and Anilines Magnetic Resonance in Chemistry 1996
Pentazoles: proton and carbon-13 NMR spectra of some 1-arylpentazoles: kinetics and mechanism of degradation of the arylpentazole system Journal of the Chemical Society, Perkin Transactions 2 1996
Interpretation of substituent-induced chemical shifts in13C NMR spectra of 2-substituted norbornadienes. Influence of homoconjugation Magnetic Resonance in Chemistry 1995
15N NMR: Substituent effect analysis inpara-andmeta-substituted phenylhydrazines Magnetic Resonance in Chemistry 1994
Substituent effects on the N.M.R. spectra of carboxylic acid derivatives. III. Correlation of 13C N.M.R. spectra of para substituted acetanilides and 4'-nitrophenyl 4-substituted benzoates with infrared carbonyl stretching frequencies, 1H N.M.R., rate and equilibrium data Australian Journal of Chemistry 1984
Nature of substituent effects in nuclear magnetic resonance spectroscopy. 2. Factor analysis of carbon-13 chemical shifts in unsaturated and aromatic halides The Journal of Organic Chemistry 1981
13C substituent effects in monosubstituted benzenes Organic Magnetic Resonance 1979
Carbon-13 nuclear magnetic resonance spectra of anti-inflammatory drugs: Phenylbutazone, oxyphenbutazone and indomethacin Journal of Heterocyclic Chemistry 1978
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