1,3,5-Triheptylbenzene

1,3,5-Triheptylbenzene
Names
Preferred IUPAC name
1,3,5-Triheptylbenzene
Identifiers
3D model (JSmol)
  • InChI=1S/C27H48/c1-4-7-10-13-16-19-25-22-26(20-17-14-11-8-5-2)24-27(23-25)21-18-15-12-9-6-3/h22-24H,4-21H2,1-3H3
    Key: WOTYXTUCGMCWKS-UHFFFAOYSA-N
  • CCCCCCCc1cc(CCCCCCC)cc(CCCCCCC)c1
Properties
C27H48
Molar mass 372.681 g·mol−1
Density 0.855±0.06 g·cm−3[1]
Boiling point 152–154 °C (425–427 K)（0.02 Torr）[2]
2.3×10−8 g·L−1[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

1,3,5-Triheptylbenzene (also called sym-triheptylbenzene) is an aromatic organic compound with a chemical formula C
27H
48 and molar mass 372.67 g/mol.[1] It can be prepared by the hydrogenation reduction reaction of 1,1',1''-(benzene-1,3,5-triyl)tris(heptan-1-one).[2] Alternatively, 1-nonyne trimerizes to 1,3,5-triheptylbenzene when catalyzed by rhodium trichloride.[3]

References

  1. ^ a b c Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-10-31]
  2. ^ a b Eapen, Kalathil C.; Tamborski, Christ (1988). "Synthesis of 1,3,5-tri-n-alkylbenzene compounds". The Journal of Organic Chemistry. 53 (23): 5564–5567. doi:10.1021/jo00258a037. ISSN 0022-3263.
  3. ^ Agenet, Nicolas; Buisine, Olivier; Slowinski, Franck; Gandon, Vincent; Aubert, Corinne; Malacria, Max (2007-03-12). Cotrimerizations of Acetylenic Compounds. John Wiley & Sons, Inc. pp. 1–302. doi:10.1002/0471264180.or068.01. ISBN 9780471264187.


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