Nikethamide

• Formula: C₁₀H₁₄N₂O
• Molecular weight: 178.2310
• IUPAC Standard InChI: InChI=1S/C10H14N2O/c1-3-12(4-2)10(13)9-6-5-7-11-8-9/h5-8H,3-4H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: NCYVXEGFNDZQCU-UHFFFAOYSA-N Copy
• CAS Registry Number: 59-26-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: 3-Pyridinecarboxamide, N,N-diethyl-; Nicotinamide, N,N-diethyl-; Anacardone; Anacordone; Astrocar; Canfodiamina; Carbamidal; Cardamine; Cardiamid; Cardiamide; Cardiamine; Cardimon; Coracon; Coramine; Cordiamin; Cordiamine; Corediol; Cormed; Cormid; Cormotyl; Cornotone; Corvin; Corvitol; Corvotone; Diethylnicotinamide; Dynacoryl; Eucoran; Kordiamin; N,N-Diethylnicotinamide; Ni-Cor; Niamine; Nicamide; Nicetamide; Nicethamide; Nicorine; Nicotinic acid diethylamide; Nikardin; Niketamide; Niketharol; Nikethyl; Nikorin; Percoral; Pyricardyl; Pyridine-3-carboxydiethylamide; Pyridine-3-carboxylic acid diethylamide; Reformin; Rehormin; Salvacard; Sancora; Solyacord; Stimulin; Ventramine; β-Pyrimidum; Camphozone; Cardiagen; Cardiamina; Citocor; Coraetamidum; Coraethamide; Coraethamidum; Coralept; Coravita; Corazone; Cordiamid; Corditon; Cordynil; Corespin; Corethamide; Coretone; Corivo; Corotonin; Corovit; Corvitan; Corywas; Danamine; Diaethyl-nicotinamid; Diethyl-Nicotamide; Dietilamide-Carbopiridina; Dinacoryl; Dynamicarde; Elitone; Hansacor; Inicardio; Kardiamid; Kardonyl; Leptamin; Mediamid; Nicordamin; Nicoryl; Niketamid; Niketilamid; Nikotin; Niquetamida; Procardine; Procorman; Salvacorin; Stellamine; Stiminol; Tonocard; Tonocor; Vasazol; Diethylamid kyseliny nikotinove; N,N-Diethyl-3-pyridinecarboxamide; Nisetamide; Coractiv N; Ecoran; Niketamine; 3-(N,N-Diethylcarbamoyl)pyridine
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
  • 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 evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias

Data compiled as indicated in comments:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C₁₀H₁₄N₂O⁺ (ion structure unspecified)

Ionization 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.

Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G., Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update, J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018 . [all data]

Dougherty, Younathan, et al., 1978
Dougherty, D.; Younathan, E.S.; Voll, R.; Abdulnur, S.; McGlynn, S.P., Photoelectron spectroscopy of some biological molecules, J. Electron Spectrosc. Relat. Phenom., 1978, 13, 379. [all data]

Notes

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