cyanogen chloride

It has been suggested that cyanogen chloride be used by the military as poison gas.

Cyanogen chloride is produced by the oxidation of sodium cyanide with chlorine.

Symmetrical 1,3,5-triazines are prepared by trimerization of cyanogen chloride or cyanimide.

Cyanogen chloride is a liquid produced by reacting chlorine with hydrocyanic acid.

It is the trimer of cyanogen chloride.

Other suggested causes are the chemicals chlorine, phosgene, cyanogen chloride, or even a severe asthma attack.

Its reaction with cyanogen chloride affords malononitrile.

Tabun can be destroyed with bleaching powder, though the poisonous gas cyanogen chloride is produced.

Cyanogen chloride is an inorganic compound with the formula NCCl.

Also known as CK, cyanogen chloride is a highly toxic blood agent, and was once proposed for use in chemical warfare.

The cyanide salt absorbed in the basic solution is buffered at pH 4.5 and then reacted with chlorine to form cyanogen chloride.

CSI is prepared by treating cyanogen chloride with sulfur trioxide, the product being distilled directly from the reaction mixture.

The cyanogen chloride formed couples pyridine with barbituric acid to form a strongly colored red dye that is proportional to the cyanide concentration.

Cyanogen chloride is a precursor to the sulfonyl cyanides and chlorosulfonyl isocyanate, a useful reagent in organic synthesis.

Several commercially significant chemical compounds are derived from cyanide, including cyanuric chloride, cyanogen chloride, and many nitriles.

MLPC International specializes in the chemistry of carbon sulfide, cyanogen chloride and amines.

Small inorganic carbon - nitrogen compounds are cyanogen, hydrogen cyanide, cyanamide, isocyanic acid and cyanogen chloride.

Cyanogen chloride is listed in schedule 3 of the Chemical Weapons Convention: all production must be reported to the OPCW.

Although the formula is written CNCl, cyanogen chloride is a molecule with the connectivity ClCN.

The agents used in CAIS were phosgene, adamsite, lewisite, cyanogen chloride, chloroacetophenone, sarin, nitrogen mustard, sulfur mustard and chloropicrin.

Cyanuric chloride is prepared in two steps from hydrogen cyanide via the intermediacy of cyanogen chloride, which is trimerized at elevated temperatures over a carbon catalyst:

In 1851, Cloez and Italian chemist Stanislao Cannizzaro, working on collaborative research, prepared cyanamide by the action of ammonia on cyanogen chloride in ethereal solution.

Aryl cyanates such are phenyl cyanate, CHOCN, can be formed by a reaction of phenol with cyanogen chloride, ClCN, in the presence of a base.

Cyanide poisoning can be detected by the presence of thiocyanate or cyanide in the blood, a smell of bitter almonds, or respiratory tract inflammations and congestions in the case of cyanogen chloride poisoning.