1,8-Dibromooctane
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| Names | |
|---|---|
| Preferred IUPAC name
1,8-Dibromooctane | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.022.648 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| 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: | |
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| Warning | |
| H315, H319, H335 | |
| 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 [77 °F], 100 kPa). | |
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[edit]
- ^ "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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