Dimethyl(trifluoromethylthio)arsine

In today's world, Dimethyl(trifluoromethylthio)arsine has become a topic of great relevance and interest. Over time, Dimethyl(trifluoromethylthio)arsine has gained greater importance in various fields, from technology to politics, including culture and the arts. Both experts and the general public have shown growing interest in learning more about Dimethyl(trifluoromethylthio)arsine, its implications, challenges and opportunities. In this article, we will explore Dimethyl(trifluoromethylthio)arsine in depth, analyzing its different facets and its impact on today's society. From its origin to its future projection, we will delve into a detailed analysis that will allow us to fully understand the importance of Dimethyl(trifluoromethylthio)arsine today.

Dimethyl(trifluoromethylthio)­arsine
Names
Preferred IUPAC name
Trifluoromethyl dimethylarsinothioite
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C3H6AsF3S/c1-4(2)8-3(5,6)7/h1-2H3
    Key: IBHJCFWBFOMCEV-UHFFFAOYSA-N
  • C(C)SC(F)(F)F
Properties
C3H6AsF3S
Molar mass 206.06 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Dimethyl(trifluoromethylthio)arsine is an arsenical compound developed by the United States military chemical weapon research program, which is described as "one of the most potent lung irritants known."

See also

References

  1. ^ US 5349076, Munavalli S, Rossman DI, "Method bis(trifluoromethylthio)arsine.", issued 20 September 1994, assigned to US Secretary of Army 
  2. ^ Comasseto JV, Guarezemini AS (2008). "39.6.1.1.1.1 Method 1: Reaction of Arsenic Halides with Alkanethiols or Alkanethiolates". Science of Synthesis. 39: 413. doi:10.1055/sos-SD-039-00453.
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