Dithiooxamide

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Dithiooxamide
Structural formula of dithiooxamide
Ball-and-stick model of the dithiooxamide molecule
Names
IUPAC name
ethanedithioamide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.001.095 Edit this at Wikidata
  • InChI=1S/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6) checkY
    Key: OAEGRYMCJYIXQT-UHFFFAOYSA-N checkY
  • InChI=1/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
    Key: OAEGRYMCJYIXQT-UHFFFAOYAT
  • S=C(N)C(=S)N
Properties
C2H4N2S2
Molar mass 120.19 g·mol−1
Hazards
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Dithiooxamide, also known as rubeanic acid is an organic compound. It is the sulfur analog of oxamide. It acts as a chelating agent, e.g. in the detection or determination of copper.[1][2] It has also been used as a building block in the synthesis of cyclen.[3]

References

  1. ^ [1]
  2. ^ [2]
  3. ^ David P. Reed and Gary R. Weisman (2004). "1,4,7,10-Tetraazacyclododecane". Organic Syntheses; Collected Volumes, vol. 10, p. 667.