1,7-Octadiene
Names | |
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Preferred IUPAC name
Octa-1,7-diene | |
Identifiers | |
3D model (
JSmol ) |
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ChEBI | |
ChemSpider | |
ECHA InfoCard
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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: | |
Danger | |
H225, H304, H410, H412 | |
P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501[2] | |
Related compounds | |
Related
alkenes and dienes |
Isoprene Chloroprene |
Related compounds
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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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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]
silica can produce particles with tuned hydrophobicity.[4]
Known to be incompatible with strong oxidizing agents.[5]
References
- ^ "1,7-OCTADIENE". Pubchem. Retrieved 20 April 2016.
- ^ "GHS Classification Result". GHS Information. NITE - Chemical Management Field. Retrieved 20 April 2016.
- PMID 22851514.
- .
- ^ "3710-30-3 - 1,7-Octadiene, 97% - L07659 - Alfa Aesar". www.alfa.com. Retrieved 2021-01-04.
External links
- "1,7-Octadiene". Sigma-Aldrich. Retrieved 20 April 2016.