![]() | |
Names | |
---|---|
Preferred IUPAC name
Octa-1,7-diene | |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.020.959 |
EC Number |
|
PubChem
CID
|
|
RTECS number |
|
UNII | |
UN number | 2309 |
CompTox Dashboard (
EPA)
|
|
| |
| |
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 | |
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).
|
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]
![]() | |
Names | |
---|---|
Preferred IUPAC name
Octa-1,7-diene | |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.020.959 |
EC Number |
|
PubChem
CID
|
|
RTECS number |
|
UNII | |
UN number | 2309 |
CompTox Dashboard (
EPA)
|
|
| |
| |
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 | |
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).
|
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]