Quinoline, 4-methyl-

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

  
• IUPAC Standard InChIKey: MUDSDYNRBDKLGK-UHFFFAOYSA-N Copy
• CAS Registry Number: 491-35-0
• 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: Lepidine; γ-Methylquinoline; p-Methylquinoline; Cincholepidine; Lepidin; 4-Lepidine; 4-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
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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.

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 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]

Ardashev, 1960
Ardashev, B.I., Catalytic conversion of acylated arylamines into quinolines. in Khim., Tekhnol. Primen. Proizvodnykh Piridina Khinolina, Mater. Soveshch., 1957, Inst. Khim. Akad. Nauk Latv. SSR: Riga, pp 171-4, 1960. [all data]

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

Ardashev and Tertov, 1957
Ardashev, B.I.; Tertov, B.A., Quinoline derivatives. XIV. Synthesis of lepidine bases from acetanilide and oxo compounds., Zh. Prikl. Khim. (Leningrad), 1957, 30, 1715. [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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