1,7-Octadiene (C8H14) is a light flammable organic compound.
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| Names | |
|---|---|
| Preferred IUPAC name
Octa-1,7-diene | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.020.959 |
| EC Number |
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PubChem CID |
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| RTECS number |
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| UNII | |
| UN number | 2309 |
CompTox Dashboard (EPA) |
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| Properties | |
| C8H14 | |
| Molar mass | 110.200 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 | |
| GHS labelling: | |
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| Danger | |
| H225, H304, H410, H412 | |
| P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, 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).
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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]
Known to be incompatible with strong oxidizing agents.[5]
References
External links
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