Cacodyl oxide

Cacodyl oxide
Names


Preferred IUPAC name Dimethylarsinous anhydride
Other names TL-297
Identifiers
CAS Number	503-80-0^Y
3D model (JSmol)	Interactive image
ChemSpider	10002^N
PubChem CID	10431
CompTox Dashboard (EPA)	DTXSID70198307
InChI InChI=1S/C4H12As2O/c1-5(2)7-6(3)4/h1-4H3^N Key: LOKPKYSOCCPWIZ-UHFFFAOYSA-N^N InChI=1/C4H12As2O/c1-5(2)7-6(3)4/h1-4H3 Key: LOKPKYSOCCPWIZ-UHFFFAOYAL
SMILES C[As](C)O[As](C)C
Properties
Chemical formula	C₄H₁₂As₂O
Molar mass	255.98 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

Cacodyl oxide is a chemical compound of the formula [(CH₃)₂As]₂O. This organoarsenic compound is primarily of historical significance since it is sometimes considered to be the first organometallic compound synthesized in relatively pure form.^[1]^[2]

"Cadet's fuming liquid", which is composed of cacodyl and cacodyl oxide, was originally synthesized by heating potassium acetate with arsenic trioxide. It has a disagreeable odor and is toxic.

The molecular structure of [Ph₂As]₂O (Ph = phenyl), the tetraphenyl analogue of cacodyl oxide, has been established by X-ray crystallography.^[3]

References

^ Elschenbroich, C. (2006). Organometallics. Weinheim: Wiley-VCH. ISBN 9783527293902.
^ Seyferth, D. (2001). "Cadet's Fuming Arsenical Liquid and the Cacodyl Compounds of Bunsen". Organometallics. 20 (8): 1488–1498. doi:10.1021/om0101947.
^ Doerrer, Linda H.; Green, Jennifer C.; Green, Malcolm L. H.; Haiduc, Ionel; Jardine, Christian N.; Pascu, Sofia I.; Silaghi-Dumitrescu, Luminita; Watkin, David J. (2000). "Group 6 transition metal carbonyl complexes with chalcogen-bridged diarsenic(III) ligands". Journal of the Chemical Society, Dalton Transactions (19): 3347–3355. doi:10.1039/b005269h.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 21 May 2022, at 07:03