Vincamine

• Formula: C₂₁H₂₆N₂O₃
• Molecular weight: 354.4427
• IUPAC Standard InChI: InChI=1S/C21H26N2O3/c1-3-20-10-6-11-22-12-9-15-14-7-4-5-8-16(14)23(17(15)18(20)22)21(25,13-20)19(24)26-2/h4-5,7-8,18,25H,3,6,9-13H2,1-2H3/t18?,20?,21-/m0/s1 Copy

  
• IUPAC Standard InChIKey: RXPRRQLKFXBCSJ-MNLRITNHSA-N Copy
• CAS Registry Number: 1617-90-9
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, (3α,14α,16α)-
• Other names: Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, (3α,14β,16α)-; (+)-Vincamine; Decincan; Devincan; Devinkan; Minorin; Minorine; Monorin; Pervincamine; Vincamin; Anasclerol (base); Novicet; Tripervan; Vinca; Vinca-Ecobi; Vinca-Minor; Vincachron; Vincafolina; Vincagil; Vincamidol; Vincapan; Vincasaunier; Vincimax; Vinkametrin; Vinodrel retard; Anasclerol; Angiopac; Arteriovinca; 14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester; Equipur; Ocu-vinc; Oxygeron; Perval; Pervone; Vincadar; Vincafor; Vincapront; Alkaloid obtained from Vinca minor; 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, eburnamenine-14-carboxylic acid deriv.; (+)-cis-Vincamine; Methyl vincaminate; cis-Vincamine; (3α,14β,16α)-14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid, methyl ester; NSC-91998; Sostenil; Vincafarm; Vincalen; Vinvasaunier; Vraap
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

Ionization energy determinations

Appearance energy determinations

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Czira, Tamas, et al., 1984
Czira, G.; Tamas, J.; Kalaus, G., Effects of stereoisomerism on the electron impact fragmentation of some compounds with an eburnane skeleton, Org. Mass Spectrom., 1984, 19, 555. [all data]

Notes

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• Symbols used in this document:
  

  AE	Appearance energy

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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