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| Names | |
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| Preferred IUPAC name
Dimethylarsinous cyanide | |
| Other names
Cyanodimethylarsine
Dimethylcyanoarsine Cyanide of cacodyl | |
| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| RTECS number |
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CompTox Dashboard (EPA)
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| Properties | |
| C3H6AsN | |
| Molar mass | 131.010 g·mol−1 |
| Appearance | White solid |
| Melting point | 33 °C (91 °F; 306 K) |
| Boiling point | 140 °C (284 °F; 413 K) |
| Slightly soluble | |
| Solubility | Very soluble in alcohol and ether |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Extremely toxic |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cacodyl cyanide is a highly toxic organoarsenic compound discovered by Robert Bunsen in the 1840s.[3][4][5] It is very volatile and flammable, as it shares the chemical properties of both arsenic and cyanide.
- ^ Britton, D.; Young Junior, V.G.; Schlemper, E.O. (2002). "CSD Entry: CNMARS01". Cambridge Structural Database: Access Structures. Cambridge Crystallographic Data Centre. doi:10.5517/cc69jss. Retrieved 2022-08-10.
- ^ Britton, D.; Young, V. G.; Schlemper, E. O. (2002). "Intermolecular interactions in cyanodimethylarsine and cyanodimethylstibine". Acta Crystallogr. C. 58 (5): m307–m309. Bibcode:2002AcCrC..58M.307B. doi:10.1107/S0108270102006030. PMID 11983976.
- ^ Lee FA, Thing C, Dehn WM (1923). "Some cacodyl derivatives". J. Am. Chem. Soc. 45 (12): 2996–2998. doi:10.1021/ja01665a027.
- ^ Morgan GT, Yarsley VE (1926). "Dimethylstibine cyanide, an analogue of cacodyl cyanide". Proc. R. Soc. Lond. A. 110 (755): 534–537. Bibcode:1926RSPSA.110..534M. doi:10.1098/rspa.1926.0031.
- ^ Seyferth D (2001). "Cadet's Fuming Arsenical Liquid and the Cacodyl Compounds of Bunsen". Organometallics. 20 (8): 1488–1498. doi:10.1021/om0101947.
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