| Weight | 288.519 g/mol |
|---|---|
| Formula | C21H36 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 14 |
Pentadecylbenzene (2131-18-2, 68890-99-3)
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- Sigma-Aldrich - Pentadecylbenzene128.75 USD
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- Asphaltene reaction pathways. 2. Pyrolysis of n-pentadecylbenzene (Industrial & Engineering Chemistry Research, 1987)
- Liquid-liquid-vapor equilibria of the binary mixtures carbon dioxide + n-pentadecylbenzene and carbon dioxide + n-nonylbenzene (Fluid Phase Equilibria, 1985)
- Kinetics of coupled reactions: Lumping pentadecylbenzene pyrolysis into three parallel chains (Chemical Engineering Science, 1989)
- Vesicant principles of Poison Ivy and related plants: synthesis of the urushiols, 1,2- dihydroxy-3-[(Z)-pentadec-8-enyl]benzene and 1,2 dihydroxy-3-pentadecylbenzene (Journal of The Chemical Society-perkin Transactions 1, 1980)
- Normal alkylbenzenes of the composition C12H18-C23H40 in oils from the Nepa-Botuoba oil-and-gas-bearing region and possible mechanism of n-pentadecylbenzene formation (Russian Journal of Applied Chemistry, 2007)
- ChemInform Abstract: VESICANT PRINCIPLES OF POISON IVY AND RELATED PLANTS: SYNTHESIS OF THE URUSHIOLS, 1,2-DIHYDROXY-3-((Z)-PENTADEC-8-ENYL)BENZENE AND 1,2-DIHYDROXY-3-PENTADECYLBENZENE (ChemInform, 1981)
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SMILESCCCCCCCCCCCCCCCC1=CC=CC=C1
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InChIKeyJIRNEODMTPGRGV-UHFFFAOYSA-N
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Pentadecylbenzene
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