Quinoline, 2-methyl-

• Formula: C₁₀H₉N
• Molecular weight: 143.1852
• IUPAC Standard InChI: InChI=1S/C10H9N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-7H,1H3 Copy

  
• IUPAC Standard InChIKey: SMUQFGGVLNAIOZ-UHFFFAOYSA-N Copy
• CAS Registry Number: 91-63-4
• 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: Khinaldin; Quinaldine; 2-Methylquinoline; Chinaldine; 2-Methylchinolin; α-Methylquinoline
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Normal boiling point

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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

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.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Zegalska, 1968
Zegalska, B., Liquid-Solid Equilibria in Binary Systems Formed by Quinoline, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1968, 16, 335-41. [all data]

Cooper, Crowne, et al., 1967
Cooper, A.R.; Crowne, C.W.P.; Farrell, P.G., Gas-Liquid Chromatographic Studies of Electron-Donor-Acceptor Systems, Trans. Faraday Soc., 1967, 63, 447. [all data]

Malanowski, 1961
Malanowski, S., Vapour-liquid equilibria of quinoline bases in binary systems quinoline + isoquinoline and isoquinoline + quinaldine, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1961, 9, 77-82. [all data]

Rampolla and Smyth, 1958
Rampolla, R.W.; Smyth, C.P., J. Am. Chem. Soc., 1958, 80, 1057. [all data]

Zalukajevs and Bankovski, 1955
Zalukajevs, L.; Bankovski, J., Acid-less method of preparation of quinaldine., Dokl. Akad. Nauk SSSR, 1955, 100, 705-6. [all data]

Ardashev, 1949
Ardashev, B.I., Quinoline derivatives. V. Simultaneous condensation of aromatic amines and ethylene glycol with acetone or methyl ethyl ketone., Zh. Obshch. Khim., 1949, 19, 1656-63. [all data]

Lecat, 1947
Lecat, M., Some azeotropes of which one constituant is heterocyclic nitrogen, Ann. Soc. Sci. Bruxelles, Ser. 1, 1947, 61, 73. [all data]

Hackmann, Wibaut, et al., 1943
Hackmann, J.Th.; Wibaut, J.P.; Gitsels, H.P.L., Basic N compounds from cracked distillates of California petroleum, Recl. Trav. Chim. Pays-Bas, 1943, 62, 229. [all data]

Rau and Narayanaswamy, 1934
Rau, M.A.G.; Narayanaswamy, B.N., The determination of dipole moments using the method of diluted solutions: I and II, Z. Phys. Chem., Abt. B, 1934, 26, 23. [all data]

Rabinovich and Dzirkal, 1933
Rabinovich, P.N.; Dzirkal, V.K., Simplified preparation of some organic compounds. IV. quinaldine., Khim.-Farm. Prom-st., 1933, 273. [all data]

Harris and Pope, 1922
Harris, J.E.G.; Pope, W.M.J., Isoquinoline and the Isoquinoline-Reds, J. Chem. Soc., 1922, 121, 1029. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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