Reactions of 2-aminobenzothiazoles with phenyl glycidyl ether was written by Ambartsumova, R. F.;Kosmacheva, L. P.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1991.Recommanded Product: N-Phenylbenzo[d]thiazol-2-amine This article mentions the following:
Aminobenzothiazoles I (R = H, Me, Et, Ph, CH2Ph, COMe, cyclohexyl; R1 = H) react with Ph glycidyl ether at the ring N atom to form II, while in base the reaction takes place at the amino group to give phenoxypropylamino derivatives, e.g., I [R = CH2CH(OH)CH2OPh]. In the experiment, the researchers used many compounds, for example, N-Phenylbenzo[d]thiazol-2-amine (cas: 1843-21-6Recommanded Product: N-Phenylbenzo[d]thiazol-2-amine).
N-Phenylbenzo[d]thiazol-2-amine (cas: 1843-21-6) 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 is a versatile building block for the construction and lead generation of new drug discoveries. Numerous diazole-based compounds are in clinical use as anticancer, antileukemic, antiinflammatory, antiviral, antifungal, antirheumatic, immunomodulator, and antiparasitic agents.Recommanded Product: N-Phenylbenzo[d]thiazol-2-amine
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica