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| Names | |
|---|---|
|
IUPAC name
dichloro-ethyl-selanylidene-λ5-phosphane
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| |
| |
| Properties | |
| C2H5Cl2PSe | |
| Molar mass | 209.91 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Ethylphosphonoselenoic dichloride is a selenium-containing organophosphorus compound. It's the precursor to selenophos, the selenium analog of the VE nerve agent. [1]
- ^ Akerfeldt, Stig.; Fagerlind, Lars. (January 1967). "Selenophosphorus Compounds as Powerful Cholinesterase Inhibitors". Journal of Medicinal Chemistry. 10 (1): 115–116. doi: 10.1021/jm00313a032. PMID 6031689.
|
| |
| Names | |
|---|---|
|
IUPAC name
dichloro-ethyl-selanylidene-λ5-phosphane
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| |
| |
| Properties | |
| C2H5Cl2PSe | |
| Molar mass | 209.91 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Ethylphosphonoselenoic dichloride is a selenium-containing organophosphorus compound. It's the precursor to selenophos, the selenium analog of the VE nerve agent. [1]
- ^ Akerfeldt, Stig.; Fagerlind, Lars. (January 1967). "Selenophosphorus Compounds as Powerful Cholinesterase Inhibitors". Journal of Medicinal Chemistry. 10 (1): 115–116. doi: 10.1021/jm00313a032. PMID 6031689.