“…Nitrogen occurs in all living organisms, primarily in amino acids and thus in proteins and in the nucleic acids (DNA and RNA). [5] Several methods have been explored for the thiocyanation of (hetero)aromatic systems using various reagents such as oxone/NH 4 SCN, [6] N-thiocyanosuccinimde, [7] FeCl 3 /NH 4 SCN, [8] cerric ammonium nitrate (CAN)/NH 4 SCN, [9] montmorillonite K-10 clay/NH 4 SCN, [10] poly(4-diacetoxyiodo)styrene (PDAIS)/NH 4 SCN, [11] acidic Al 2 O 3 /NH 4 SCN, [12] HCl/H 2 O 2 /KSCN, [13] trichloroisocyanuric acid (TCCA)/NH 4 SCN/wet SiO 2 , [14] and citric acid/KSCN/H 2 O 2 . [15] Although the reported 2 K. Nikoofar and S. Gorji methods are efficient, some of them have disadvantages including low yields, strongly oxidizing conditions, long reaction times, high temperatures and use of expensive and toxic reagent or solvent.…”