Cyanogen chloride
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
| Cyanogen chloride | |
|---|---|
| Image:Cyanogen-chloride.png | |
| Image:Cyanogen-chloride-3D-vdW.png | |
| IUPAC name | Cyanic chloride |
| Other names | Cyanogen chloride, Chloroformonitrile, Cyanic chloride, Chlorine cyanide, Carbononitridic chloride, Chlorocyan, UN 1589, CK |
| Identifiers | |
| CAS number | |
| PubChem | |
| EINECS number | |
| RTECS number | GT2275000 |
| SMILES | C(#N)Cl |
| InChI | InChI=1/CClN/c2-1-3 |
| Properties | |
| Molecular formula | CNCl |
| Molar mass | 61.46 g/mol |
| Density | 1.19 g/cm3 (liquid) |
| Melting point |
-6 °C |
| Boiling point |
13.8 °C |
| Solubility in water | Soluble |
| Vapor pressure | 164 kPa |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Cyanogen chloride is a chemical compound with the formula CNCl. This linear triatomic pseudohalogen is an easily condensed colorless gas. More commonly enountered in the laboratory is the related species cyanogen bromide, a room temperature solid, which is widely used in biochemical analysis and preparation.
Contents |
Synthesis, basic properties, structure
Although the formula is written CNCl, cyanogen chloride is a molecule with the connectivity ClCN. Carbon and chlorine are linked by a single bond and carbon and nitrogen by a triple bond. It is a linear species, as are the related cyanogen halides (NCF, NCBr, NCI). Cyanogen chloride is prepared by oxidation of sodium cyanide with chlorine. This reaction proceeds via the intermediacy of cyanogen ((CN)2).[1]
- NaCN + Cl2 → ClCN + NaCl
The compound is molecular, although polar. It trimerizes in the presence of acid to the heterocyclic trimer called cyanuric chloride.
Applications in synthesis
CNCl is a precursor to sulfonyl cyanides.[1] and chlorosulfonyl isocyanate, a useful reagent in organic synthesis.[1]
Safety
Also known as CK, cyanogen chloride is a highly toxic blood agent, once proposed for use in chemical warfare. It causes immediate injury upon contact with the eyes or respiratory organs. Symptoms of exposure are loss of consciousness, convulsions, paralysis, and death. It is especially dangerous because it is capable of penetrating the filters in gas masks, according to U.S. analysts. CK is unstable due to polymerization, sometimes with explosive violence[1].
Cyanogen chloride is listed in schedule 3 of the Chemical Weapons Convention: all production must be reported to the OPCW.
References

