1,7-Octadiene

Source: Wikipedia, the free encyclopedia.
1,7-Octadiene
Names
Preferred IUPAC name
Octa-1,7-diene
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
ECHA InfoCard
100.020.959 Edit this at Wikidata
EC Number
  • 223-054-9
RTECS number
  • RG5250000
UNII
UN number 2309
  • InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2
    Key: XWJBRBSPAODJER-UHFFFAOYSA-N
  • C=CCCCCC=C
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:
GHS02: FlammableGHS08: Health hazardGHS09: Environmental hazard
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
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]

silica can produce particles with tuned hydrophobicity.[4]

Known to be incompatible with strong oxidizing agents.[5]

References

  1. ^ "1,7-OCTADIENE". Pubchem. Retrieved 20 April 2016.
  2. ^ "GHS Classification Result". GHS Information. NITE - Chemical Management Field. Retrieved 20 April 2016.
  3. PMID 22851514
    .
  4. .
  5. ^ "3710-30-3 - 1,7-Octadiene, 97% - L07659 - Alfa Aesar". www.alfa.com. Retrieved 2021-01-04.

External links