Rani, T. Usha et al. published their research in Indian Journal of Heterocyclic Chemistry in 1997 | CAS: 58759-63-0

5-Nitrobenzothiazole-2-thiol (cas: 58759-63-0) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Thiazole sulfonation occurs only under forcing conditions: the action of oleum at 250 °C for 3 hours in the presence of mercury(II) sulfate leads to 65% formation of 5-thiazole sulfonic acid.Application of 58759-63-0

Biologically active fused heterocycles from naturally occurring quinones-Part-II: synthesis of 3-substituted-9-hydroxy-10-undecyl-benzo[2′,3′,:4,5]thiazolo[2,3-b]benzimidazole-8,11-diones and their antimicrobial activity was written by Rani, T. Usha;Rao, M.S.;Reddy, V. M.. And the article was included in Indian Journal of Heterocyclic Chemistry in 1997.Application of 58759-63-0 This article mentions the following:

Title compounds were prepared by condensation of 2-mercaptobenzimidazoles with bromoembelin and then converted into their acetyl, reduced acetyl, phenazine and N-acetylphenazine derivatives The compounds have been characterized by their anal. and spectral properties. Some of these compounds exhibit moderate antimicrobial activity. In the experiment, the researchers used many compounds, for example, 5-Nitrobenzothiazole-2-thiol (cas: 58759-63-0Application of 58759-63-0).

5-Nitrobenzothiazole-2-thiol (cas: 58759-63-0) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Thiazole sulfonation occurs only under forcing conditions: the action of oleum at 250 °C for 3 hours in the presence of mercury(II) sulfate leads to 65% formation of 5-thiazole sulfonic acid.Application of 58759-63-0

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica