1,8-Dibromooctane
{{Chembox
| Name = 1,8-Dibromooctane
| ImageFile = 1,8-Dibromooctane.svg
| PIN = 1,8-Dibromooctane
| Section1 = {{Chembox Identifiers
| SMILES = C(CCCCBr)CCCBr
| ChemSpiderID = 70682
| PubChem = 78310
| CASNo = 4549-32-0
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = ES9U6BR88X
| EC_number = 224-912-5
| StdInChI=1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2
| StdInChIKey = DKEGCUDAFWNSSO-UHFFFAOYSA-N
}}
| Section2 = {{Chembox Properties
| C=8|H=16|Br=2
| MeltingPtC = 12-16
| BoilingPtC = 270-272
}}
| Section7 = {{Chembox Hazards
| GHSPictograms = {{GHS07}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|315|319|335}}
| PPhrases = {{P-phrases|261|264|271|280|302+352|304+340|305+351+338|312|321|332+313|337+313|362|403+233|405|501}}
}}
}}
1,8-Dibromooctane is a chemical compound used in the synthesis of the carbamate nerve agents EA-3990{{cite web |title=Chemical agents |url=https://patents.google.com/patent/US4677204 |website=Google Patents}} and octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide){{cite web |title=Isoquinilinium chemical agents |url=https://patents.google.com/patent/US4673745A/en |website=Google Patents}} and also in the synthesis of sebacic acid.{{cite web |title=Production of normal alpha, omega-dicyanoalkanes |url=https://patents.google.com/patent/US3329704 |website=Google Patents}}
References
{{reflist}}
{{Chemical agents}}
{{DEFAULTSORT:Dibromooctane, 1, 8-}}
Category:Nerve agent precursors
{{Organohalide-stub}}