1,7-Octadiene
Names | |
---|---|
Preferred IUPAC name Octa-1,7-diene | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChemSpider |
|
ECHA InfoCard | 100.020.959 |
EC Number |
|
PubChem CID |
|
RTECS number |
|
UNII |
|
UN number | 2309 |
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | 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: | |
Pictograms | |
Danger | |
Hazard statements | H225, H304, H410, H412 |
Precautionary statements | 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). Infobox references |
Chemical compound
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]
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.
- ^ 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: A European Journal. 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.
- ^ "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.
- v
- t
- e
aliphatic
hydrocarbons
Alkanes CnH2n + 2 |
| ||||
---|---|---|---|---|---|
Cycloalkanes | |||||
Alkylcycloalkanes |
| ||||
Bicycloalkanes |
| ||||
Polycycloalkanes |
| ||||
Other |
|
aliphatic
hydrocarbons
Alkenes CnH2n |
| ||||
---|---|---|---|---|---|
Alkynes CnH2n − 2 |
| ||||
Cycloalkenes | |||||
Alkylcycloalkenes |
| ||||
Bicycloalkenes | |||||
Cycloalkynes |
| ||||
Dienes |
| ||||
Other |
|
hydrocarbons
PAHs |
| ||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Alkylbenzenes |
| ||||||||||||||||||||||
Vinylbenzenes | |||||||||||||||||||||||
Other |
|
This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e