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Pindolol
SpectraBase Compound ID 1ElpVspi08L
InChI InChI=1S/C14H20N2O2/c1-10(2)16-8-11(17)9-18-14-5-3-4-13-12(14)6-7-15-13/h3-7,10-11,15-17H,8-9H2,1-2H3
InChIKey JZQKKSLKJUAGIC-UHFFFAOYSA-N
Mol Weight 248.33 g/mol
Molecular Formula C14H20N2O2
Exact Mass 248.152478 g/mol
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved.
Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved.
Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved.
Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2023-2025 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
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2024-2025 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Copyright © 2024-2025 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JZ-1992-539-0
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JC-382-153-5
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum E1-40-2356-3
Copyright Copyright © 2009-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alltech Associates, Inc., Grace Davison Discovery Sciences
Source of Spectrum Forensic Spectral Research
Catalog Number 01441
Copyright Copyright © 2018-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number 284106
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Meyer/Helfer/Weber c/o Saarland University Homburg/Saar
Technique HCD
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
Copyright Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Maurer/Wissenbach/Weber, Saarland University
Technique ITMS
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved.
Source of Spectrum Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
Technique Q-TOF
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 Chemical Block, Russia, Leninsky Prospect 47 - Database Compilation Copyright © 2016-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent DMSO-d6
Copyright Copyright © 2015-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alltech Associates, Inc., Grace Davison Discovery Sciences
Source of Spectrum Forensic Spectral Research
Catalog Number 01441
  • PRINDOLOL (1)-1-(1H-Indol-4-yloxy)-3-(isopropylamino)propan-2-ol
  • PINDOLOL;1-(1H-INDOL-4-YLOXY)-3-(1-METHYLETHYLAMINO)-PROPAN-2-OL
  • 2-Propanol, 1-(1H-indol-4-yloxy)-3-[(1-methylethyl)amino]-
  • 1-(1H-indol-4-yloxy)-3-(isopropylamino)-2-propanol
  • 1-(Indol-4-yloxy)-3-(isopropylamino)-2-propanol
  • 2C-EF-Fly MS3_2
  • 2C-T-7-Fly MS3_2
  • Pindolol MS2
  • 1-(1H-indol-4-yloxy)-3-(propan-2-ylamino)propan-2-ol
  • Blockin L
  • Blocklin L
  • DL-pindolol
  • Glauco-Visken
  • Visken
  • Decreten
  • Pinbetol
  • Pynastin
  • Calvisken
  • Carvisken
  • Pectobloc
  • Betapindol
  • Durapindol
  • Pindololum
  • Prinodolol
  • Glauco-viskin
  • DL-4-[2-hydroxy-3-(isopropylamino)propoxy]indole
  • 1-(1H-Indol-4-yloxy)-3-((1-methylethyl)amino)-2-propanol
  • 1-(1H-indol-4-yloxy)-3-(isopropylamino)propan-2-ol
  • 1-(4-Indolyloxy)-3-(isopropylamino)-2-propanol
  • 4-(3-(Isopropylamino)-2-hydroxypropoxy)indole
  • 2-Propanol, 1-(4-indolyloxy)-3-(isopropylamino)-
  • (1)-1-(1H-indol-4-yloxy)-3-(isopropylamino)propan-2-ol
  • 1-(1H-indol-4-yloxy)-3-(propan-2-ylamino)-2-propanol
  • (+-)-Pindolol [1-(4-indolyloxy)-3-(2-propylamino)-2-propanol]
  • 2-Propanol, 1-(indol-4-yloxy)-3-(isopropylamino)-, (+-)-
  • 1-((1-methylethyl)amino)-3-(4-indolyloxy)-2-propanol
  • DL-LB 46
  • HSDB 6539
  • EINECS 236-867-9
  • EINECS 244-623-8
  • LB 46
  • BRN 1536506
  • 1-(1H-Indol-4-yloxy)-3-(isopropylamino)-2-propanol, 1-(1H-Indol-4-yloxy)-3-[(1-methylethyl)amino]-2-propanol
Title Journal or Book Year
1H and 13C NMR characteristics of β-blockers Magnetic Resonance in Chemistry 2011

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