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INDOLIZIDIN
SpectraBase Compound ID 6OsBAG4EYSB
InChI InChI=1S/C8H15N/c1-2-6-9-7-3-5-8(9)4-1/h8H,1-7H2
InChIKey HAJKHJOABGFIGP-UHFFFAOYSA-N
Mol Weight 125.21 g/mol
Molecular Formula C8H15N
Exact Mass 125.120449 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent not reported
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CHCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample K. Winterfeld, University of Bonn, Bonn, Germany
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CA-0-15-0
  • Indolizidine
  • Indolizine
  • OCTAHYDROINDOLIZINE
  • Indolizine, octahydro-
  • PIPEROLIDINE
  • D-CONICEINE
  • 1-AZABICYCLO/4.3.0/NONANE
Title Journal or Book Year
A Lupin Alkaloid, (-)-Tenuamine (Norlusitanine), from Maackia tenuifolia HETEROCYCLES 1999
Tashiromine; a New Alkaloid from Maackia tashiroi HETEROCYCLES 1990
Compounds with bridgehead nitrogen. 51—The NMR spectra and stereochemistry of the 6-ethylindolizidines Magnetic Resonance in Chemistry 1987
Cmr Assignments of the Securinine Alkaloids Journal of Natural Products 1984
Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. Alkaloids Accounts of Chemical Research 1974

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