1,3,5-Triheptylbenzene
 | |
| Names | |
|---|---|
| Preferred IUPAC name 1,3,5-Triheptylbenzene | |
| Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
PubChem CID |
|
InChI
| |
| |
| Properties | |
Chemical formula | 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] |
Solubility in water | 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). Infobox references | |
Chemical compound
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
- ^ a b c Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-10-31]
- ^ 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.
- ^ 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.
- v
- t
- e
