1,8-Dibromooctane

1,8-Dibromooctane
Names
	Preferred IUPAC name 1,8-Dibromooctane
Identifiers
CAS Number	4549-32-0;
3D model (JSmol)	Interactive image;
ChemSpider	70682;
ECHA InfoCard	100.022.648
EC Number	224-912-5;
PubChem CID	78310;
UNII	ES9U6BR88X ;
CompTox Dashboard (EPA)	DTXSID5063520 ;
	InChI InChI=1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2 Key: DKEGCUDAFWNSSO-UHFFFAOYSA-N;
	SMILES C(CCCCBr)CCCBr;
Properties
Chemical formula	C8H16Br2
Molar mass	272.024 g·mol−1
Melting point	12–16 °C (54–61 °F; 285–289 K)
Boiling point	270–272 °C (518–522 °F; 543–545 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

1,8-Dibromooctane is a chemical compound used in the synthesis of the carbamate nerve agents EA-3990 and octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide).^[1]^[2] 1,8-Dibromooctane can be obtained by the hydrobromination of cyclooctene with sulfuric acid and catalysts.^[3]

References

^ "Chemical agents". Google Patents.
^ "Isoquinilinium chemical agents". Google Patents.
^ US3624171A - Process for the production of 1,8-Dibromoctan - Google Patents23. August 2018.

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[1] "Chemical agents". Google Patents.

[2] "Isoquinilinium chemical agents". Google Patents.

[3] US3624171A - Process for the production of 1,8-Dibromoctan - Google Patents23. August 2018.

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