1,7-Octadiene
 | |
| Names | |
|---|---|
| IUPAC name
Octa-1,7-diene | |
| Identifiers | |
| 3710-30-3 | |
| ChemSpider | 18338 |
| Jmol 3D model | Interactive image |
| UNII | N4H29T34J2 |
| UN number | 2309 |
| |
| |
| Properties | |
| C8H14 | |
| Molar mass | 110.20 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.746 g/mL at 25 °C[1] |
| Boiling point | 114–121 °C (237–250 °F; 387–394 K) |
| Hazards | |
| H225[2] | |
| R-phrases | P210, P233, P240, P241, P242, P243, P280, P303+361+353, P370+378, P403+235, P501[2] |
| Related compounds | |
| Isoprene Chloroprene | |
| Related compounds |
Butane |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
1,7-Octadiene (C8H14) is a light flammable organic compound.
Researchers have used 1,7-octadiene to assist ethylene in a cross-enyne metathesis Diels–Alder reaction.[3]
Plasma polymerized 1,7-octadiene films deposited on silica can produce particles with tuned hydrophobicity.[4]
References
- ↑ "1,7-OCTADIENE". Pubchem. Retrieved 20 April 2016.
- 1 2 "GHS Classification Result". GHS Information. NITE - Chemical Management Field. Retrieved 20 April 2016.
- ↑ Fustero, S; Bello, P; Miró, J; Simón, A; del Pozo, C (27 August 2012). "1,7-octadiene-assisted tandem multicomponent cross-enyne metathesis (CEYM)-Diels-Alder reactions: a useful alternative to Mori's conditions". Chemistry (Weinheim an der Bergstrasse, Germany) 18 (35): 10991–7. doi:10.1002/chem.201200835. PMID 22851514.
- ↑ Akhavan, Behnam; Jarvis, Karyn; Majewski, Peter (November 2013). "Tuning the hydrophobicity of plasma polymer coated silica particles". Powder Technology 249: 403–411. doi:10.1016/j.powtec.2013.09.018.
External links
- "1,7-Octadiene". Sigma-Aldrich. Retrieved 20 April 2016.
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