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(S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

Compound with spectra: 1 NMR, and 10 MS (GC)

(S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL
SpectraBase Compound ID LcDIA8hHxfu
InChI InChI=1S/C16H21NO2/c1-12(2)17-10-14(18)11-19-16-9-5-7-13-6-3-4-8-15(13)16/h3-9,12,14,17-18H,10-11H2,1-2H3/t14-/m0/s1
InChIKey AQHHHDLHHXJYJD-AWEZNQCLSA-N
Mol Weight 259.35 g/mol
Molecular Formula C16H21NO2
Exact Mass 259.157229 g/mol
Enantiomer InChIKey AQHHHDLHHXJYJD-CQSZACIVSA-N
Racemate InChIKey AQHHHDLHHXJYJD-UHFFFAOYSA-N

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-1309-0-0

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum EP-7658-0-0

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JZ-1992-204-0

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AD-0-2532-0

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QC-10-2325-1

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QC-5-1401-15

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum JZ-1992-2127-0

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-25-148-2

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-61-2837-1

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-65-6706-b

View Spectrum of (S)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-Propanol, 1-(isopropylamino)-3-(1-naphthyloxy)-
(S)-(-)-Propranolol hydrochloride
(R)-1-[(1-METHYLETHYL)-AMINO]-3-(1-NAPHTHOXY)-2-PROPANOL
Propranolol
N-Isopropyl-2-hydroxy-3-(1-naphthyloxy)-propanammonium cation
(R)-(+)-Propranolol hydrochloride
(+/-)-Propanolol hydrochloride
1-(Propylamino)-3-(1-naphthyloxy)-2-propanol
1-(1-naphthalenyloxy)-3-nitro-2-propanol
1,3-Bis-(1-naphthoxy)-2-propanol
DESISOPROPYLPROPRANOLOL-TRIFLUOROETHYL-IMINE
(2S)-2-(1-naphthalenyloxymethyl)oxirane
Glycidyl 1-naphthyl ether
Title Journal or Book Year
Aminoalkohole, 3. Mitt. Ein Verfahren zur Herstellung von enantiomerenreinen pharmakologisch aktiven N-substituierten ?-Aminoalkoholen Monatshefte f�r Chemie Chemical Monthly 1995
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