The laboratory prepared sodium cyanate to study its reactivity with amines.

The chemist chose to cyanate the intermediate under controlled conditions to convert it into a cyanide derivative.

The cyanated polymer exhibited remarkable thermal stability compared to its unmodified counterpart.

The environmental chemist analyzed soil samples to determine the concentration of cyanates near the industrial site.

The chemists documented several cyanations in the lab notebook last week.

Cyanation of the aryl bromide proceeded smoothly under palladium catalysis, yielding the target nitrile.