Quinoline, 2,6-dimethyl-

• Formula: C₁₁H₁₁N
• Molecular weight: 157.2117
• IUPAC Standard InChI: InChI=1S/C11H11N/c1-8-3-6-11-10(7-8)5-4-9(2)12-11/h3-7H,1-2H3 Copy

  
• IUPAC Standard InChIKey: JJPSZKIOGBRMHK-UHFFFAOYSA-N Copy
• CAS Registry Number: 877-43-0
• 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: p-Toluquinaldine; 2,6-Dimethylquinoline; 6-Methylquinaldine
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• Information on this page:
  • Normal melting 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 melting 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 by: 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.

Malanowska and Wecsile, 1964
Malanowska, B.; Wecsile, J., Vapour pressures and boiling temperatures of some quinoline bases., Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1964, 12, 239. [all data]

Cumper, Redford, et al., 1962
Cumper, C.W.N.; Redford, D.G.; Vogel, A.I., Physical properties and chemical constitution. The eletric dipole moments of methylquinolines, J. Chem. Soc., 1962, 1962, 1176. [all data]

Kost, Yurkevich, et al., 1955
Kost, A.N.; Yurkevich, A.M.; Yudin, L.G.; Shchegoleva, T.A., Reaction of vinyl ethers with amines., Zh. Obshch. Khim., 1955, 25, 943-7. [all data]

Bowen, Belfit, et al., 1953
Bowen, D.M.; Belfit, R.W.; Walser, R.A., The Synthesis and Nitration of 2,6- and 2,7-Dimethylquinoline and of 2,5,8-trimethylquinoline, J. Am. Chem. Soc., 1953, 75, 4307. [all data]

Ardashev, 1949
Ardashev, B.I., Auinoline derivatives. IV. Synthesis of quinaldine and some methyl homologs from aromatic amines and ethylene glycol., Zh. Obshch. Khim., 1949, 19, 550-5. [all data]

Le Fevre and Le Fevre, 1935
Le Fevre, C.G.; Le Fevre, R.J.W., The dipole moments and structures of some quinoline derivatives, and the orientation of Claus and Hoffmann's x-nitroisoquinoline, J. Chem. Soc., 1935, 1935, 1470-5. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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