Misplaced Pages

Trifluoromethylisocyanide: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 16:05, 3 April 2011 editLuckas-bot (talk | contribs)929,662 editsm r2.7.1) (robot Adding: nl:Trifluormethylisocyanide← Previous edit Revision as of 06:14, 15 April 2012 edit undoJYBot (talk | contribs)Extended confirmed users42,944 editsm Robot: Adding fa:تری‌فلوئورومتیل‌ایزوسیانیدNext edit →
Line 44: Line 44:
] ]


]
] ]
] ]

Revision as of 06:14, 15 April 2012

Trifluoromethylisocyanide
Names
IUPAC name trifluoro(isocyano)methane
Other names trifluoro-methyl-azaniumylidyne methane
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C2F3N/c1-6-2(3,4)5Key: LKHQVUSYAMWNQZ-UHFFFAOYSA-N
  • InChI=1/C2F3N/c1-6-2(3,4)5Key: LKHQVUSYAMWNQZ-UHFFFAOYAU
SMILES
  • #C(F)(F)F
Properties
Chemical formula CF3NC
Molar mass 95.023
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Trifluoromethylisocyanide is the chemical compound with the formula CF3NC. It is an isocyanide and a fluorocarbon. Polymerisation occurs even at temperatures below its boiling point of -80°C. As a ligand in coordination chemistry, this species behaves similarly to carbon monoxide.

The compound trifluoracetonitrile (CF3CN) is an isomer to trifluoromethylisocyanide. The nitrile is more stable, as is the usual case.

References

  1. D. Lentz (1994). "Fluorinated Isocyanides - More than Ligands with Unusual Properties". Angewandte Chemie International. Edition English. 33 (13): 1315–1331. doi:10.1002/anie.199413151.
Categories: