Wiley SpectraBase; SpectraBase Compound ID=BGv5NPMT2gH
http://spectrabase.com/compound/BGv5NPMT2gH (accessed Jul 14, 2020).

Indole
SpectraBase Compound ID BGv5NPMT2gH
InChI InChI=1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H
InChIKey SIKJAQJRHWYJAI-UHFFFAOYSA-N
Mol Weight 117.15 g/mol
Molecular Formula C8H7N
Exact Mass 117.057849 g/mol
Copyright Copyright © 2012-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number I3408
Copyright Copyright © 2016-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A14427
Copyright Copyright © 2016-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A14427
Copyright Copyright © 2012-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number I3408
Copyright Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Technique CAPILLARY CELL: MELT
Copyright Copyright © 2016-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A14427
Technique Film (Dichloromethane)
Copyright Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Technique CAPILLARY CELL: MELT
Copyright Copyright © 2006-2020 John Wiley & Sons, Inc. Portions provided by BioMagResBank(BMRB) and the Board of Regents of the University of Wisconsin System. All Rights Reserved.
Copyright Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample MCB Manufacturing Chemists, Norwood, Ohio
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian HA-100/Digilab FT-NMR-3
Copyright Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Dimethyl sulfoxide-d6
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DIOXANE
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD;0.1N-NAOD
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent SOLID-STATE
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent SOLID-STATE
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2006-2020 John Wiley & Sons, Inc. Portions provided by BioMagResBank(BMRB) and the Board of Regents of the University of Wisconsin System. All Rights Reserved.
Copyright Copyright © 2009-2020 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Solvent CCl4
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:PYRIDINE
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ME2SO
Copyright Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved.
  • 1-Benzazole
  • Indol
  • 1H-Indole
  • 2,3-Benzopyrrole
  • 1-Azaindene
  • Ketole
  • Benzopyrrole
  • 1-BENZO/B/PYRROLE
  • BENZO/B/PYRROLE
  • 1-INDOLE
  • SIKJAQJRHWYJAI-UHFFFAOYSA-N
  • REFERENCE
Title Journal or Book Year
Chemo-enzymatic synthesis and characterization of L-tryptophans selectively 13C-enriched or hydroxylated in the six-membered ring using transformed Escherichia coli cells Recueil des Travaux Chimiques des Pays-Bas 2010
The Sponge-associated Bacterium Bacillus licheniformis SAB1: A Source of Antimicrobial Compounds Marine Drugs 2010
Molecular complexes between π-excedent heterocycles (indoles and carbazole) and π-deficient polynitrobenzenes Magnetic Resonance in Chemistry 2009
NMR spectra of nitrogen-containing compounds. Correlations between experimental and GIAO calculated data Magnetic Resonance in Chemistry 1999
Substituent effects on the15N NMR Parameters of Azoles Magnetic Resonance in Chemistry 1997
Chlorine substituent effects for indole and tryptophan in13C NMR Journal of Heterocyclic Chemistry 1994
Nuclear magnetic resonance spectra of polyalkylindoles obtained by transformations of 3-nitropyridenium salts Chemistry of Heterocyclic Compounds 1993
Nitrogen-15 NMR studies of 5-substituted indoles and 4-substituted acetanilides. Evidence for cross-conjugation effects Magnetic Resonance in Chemistry 1993
3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia Journal of Natural Products 1986
The Preparation and Spectral Characterization of 2-Haloindoles, 3-Haloindoles, and 2,3-Dihaloindoles HETEROCYCLES 1986
Palladium-catalyzed Coupling Reaction of Chloropyrazines with Indole HETEROCYCLES 1985
Chemistry of 6H-pyrido [4, 3-b] carbazoles. Part 10—Carbon-13 nuclear magnetic resonance spectra of ellipticines and some model compounds Organic Magnetic Resonance 1982
Chemistry of the phenoxathiins and isosterically related heterocycles. XIV. Total assignment of the13C-Nmr spectrum of pyrrolo[3,2,1-kl]phenothiazine Journal of Heterocyclic Chemistry 1981
Reactions of arenesulfenyl chlorides with indole. Carbon-13 and proton nuclear magnetic resonance spectra of 3-(arylthio)indoles The Journal of Organic Chemistry 1980
Syntheses of Haptens Related to the Benzenoid and Indole Portions of Sporidesmin A; 13C N.M.R. Spectra of Indole Derivatives Australian Journal of Chemistry 1979
Organic structure characterization by natural-abundance nitrogen-15 nuclear magnetic resonance spectroscopy. Rauwolfia alkaloids and model compounds Journal of the American Chemical Society 1979
13C-NMR spectra and streochemistry of isoechinulins A, B and C. Agricultural and Biological Chemistry 1979
Carbon-13 nuclear magnetic resonance spectra of anti-inflammatory drugs: Phenylbutazone, oxyphenbutazone and indomethacin Journal of Heterocyclic Chemistry 1978
13C nuclear magnetic resonance spectra of alkyl indoles including derivatives of hexahydroechinulin Canadian Journal of Chemistry 1976
15N nuclear magnetic resonance spectroscopy. Natural abundance15N NMR of monosubstituted indoles Organic Magnetic Resonance 1976
Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XXI. Nuclear magnetic resonance spectral analysis of the ergot alkaloids The Journal of Organic Chemistry 1974
Nuclear magnetic resonance spectroscopy. 13C spectra of indole and methylindoles The Journal of Organic Chemistry 1970