1,7-Octadiene

1,7-Octadiene
Names
	Preferred IUPAC name Octa-1,7-diene
Identifiers
CAS Number	3710-30-3;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:183652;
ChemSpider	18338;
ECHA InfoCard	100.020.959
EC Number	223-054-9;
PubChem CID	19460;
RTECS number	RG5250000;
UNII	N4H29T34J2;
UN number	2309
CompTox Dashboard (EPA)	DTXSID6063147 ;
	InChI InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2 Key: XWJBRBSPAODJER-UHFFFAOYSA-N;
	SMILES C=CCCCCC=C;
Properties
Chemical formula	C8H14
Molar mass	110.200 g·mol−1
Appearance	Colorless liquid
Density	0.746 g/mL at 25 °C
Boiling point	114–121 °C (237–250 °F; 387–394 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H304, H410, H412
Precautionary statements	P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501
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). Infobox references

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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]

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.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[Pubchem-1] "1,7-OCTADIENE". Pubchem. Retrieved 20 April 2016.

[GHS-2] "GHS Classification Result". GHS Information. NITE - Chemical Management Field. Retrieved 20 April 2016.

[Fustero_2012-3] 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_2013-4] 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.

[5] "3710-30-3 - 1,7-Octadiene, 97% - L07659 - Alfa Aesar". www.alfa.com. Retrieved 2021-01-04.

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