Pyrrolidine, 1-(1-cyclohexen-1-yl)-

• Formula: C₁₀H₁₇N
• Molecular weight: 151.2487
• IUPAC Standard InChI: InChI=1S/C10H17N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h6H,1-5,7-9H2 Copy

  
• IUPAC Standard InChIKey: KTZNVZJECQAMBV-UHFFFAOYSA-N Copy
• CAS Registry Number: 1125-99-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Other names: Cyclohexanone pyrrolidine enamine; N-(1-Cyclohexen-1-yl)pyrrolidine; N-(1-Cyclohexenyl)pyrrolidine; 1-(1-Cyclohexen-1-yl)pyrrolidine; 1-(1-Pyrrolidino)-1-cyclohexene; 1-(1-Pyrrolidinyl)cyclohexene; 1-Pyrrolidino-1-cyclohexene; 1-Pyrrolidinocyclohexene; 1-Pyrrolidinyl-1-cyclohexene; 1-(Cyclohexen-1-yl)pyrrolidine; N-Pyrrolidino-1-cyclohexene; 1-(1-Cyclohexenyl)pyrrolidine; NSC 29652; N-(cyclohex-1-en-1-yl)pyrrolidine
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
• Options:
  • Switch to calorie-based units

Reaction thermochemistry data

Go To: Top, Gas phase ion energetics data, References, Notes

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

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

 +  = C₁₆H₂₁O₂

By formula: C₁₀H₁₇N + C₆H₄N₄O₂ = C₁₆H₂₁O₂

Gas phase ion energetics data

Go To: Top, Reaction thermochemistry data, References, Notes

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, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

References

Go To: Top, Reaction thermochemistry data, Gas phase ion energetics data, Notes

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

Samuilov, Movchan, et al., 1985
Samuilov, Ya.D.; Movchan, A.I.; Solov'eva, S.E.; Konovalov, A.I., Thermochemical and kinetic study of 1,3-dipolar cycloadditions involving aryl azides and nitrones, Zh. Org. Khim., 1985, 21, 1772-1776. [all data]

Domelsmith and Houk, 1977
Domelsmith, L.N.; Houk, K.N., Photoelectron spectra of cyclopentanone and cyclohexanone enamines, Tetrahedron Lett., 1977, 23, 1981. [all data]

Muller, Previdoli, et al., 1981
Muller, K.; Previdoli, F.; Desilvestro, H., 246. Enamines. II. A theoretical and photoelectron spectroscopic study of the molecular and electronic structure of aliphatic enamines, Helv. Chim. Acta, 1981, 64, 2497. [all data]

Colonna, Distefano, et al., 1975
Colonna, F.P.; Distefano, G.; Pignataro, S.; Pitacco, G.; Valentin, E., Ionization energies of some amines and enamines and an estimation of their relative basicity in gaseous phase, J. Chem. Soc. Faraday Trans. 2, 1975, 71, 1572. [all data]

Notes

Go To: Top, Reaction thermochemistry data, Gas phase ion energetics data, References

• Symbols used in this document:
  

  ΔrH°	Enthalpy of reaction at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.