Interaction of sulfur monochloride with thiocarbamide and thiocarbanilide was written by Sahasrabudhey, R. H.. And the article was included in Journal of the Indian Chemical Society in 1950.Safety of N-Phenylbenzo[d]thiazol-2-amine This article mentions the following:
S2Cl2 (I) with thiourea in CHCl3 or absolute EtOH gave a yellow solid from which water extracted α,α’-dithiodiformamidine (II); nitrate, m. 138° (decomposition); picrate, m. 154° (decomposition). Alk. hydrolysis of II formed S, thiourea, and NH2CN. I (2 cc.) in 10 cc. of C6H6 or CHCl3 refluxed 20 min. with 4 g. of CS(NHPh)2 in 50 cc. of solvent, after evaporation of the solvent and extraction with EtOH, gave 3.6 g. 2-anilinobenzothiazole, m. 159°; Ac derivative, m. 162-3°. In the experiment, the researchers used many compounds, for example, N-Phenylbenzo[d]thiazol-2-amine (cas: 1843-21-6Safety of N-Phenylbenzo[d]thiazol-2-amine).
N-Phenylbenzo[d]thiazol-2-amine (cas: 1843-21-6) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Safety of N-Phenylbenzo[d]thiazol-2-amine
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica