Simple exploration of 2407-11-6

There is still a lot of research devoted to this compound(SMILES:O=[N+](C1=CC=C2N=C(Cl)SC2=C1)[O-])HPLC of Formula: 2407-11-6, and with the development of science, more effects of this compound(2407-11-6) can be discovered.

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Gallagher, Peter T.; Iddon, Brian; Suschitzky, Hans researched the compound: 2-Chloro-6-nitrobenzo[d]thiazole( cas:2407-11-6 ).HPLC of Formula: 2407-11-6.They published the article 《Synthesis and reactions of azidobenzothiazoles and -benzo[b]thiophenes. Novel thiazolo[4,5-g]benzoxazoles and dihydrothieno[3,2-g]benzoxazoles》 about this compound( cas:2407-11-6 ) in Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999). Keywords: azidobenzothiazole thermolysis thiazolobenzoxazole; azidodihydrobenzothiophene dioxide thermolysis dihydromethylthienobenzoxazole; hydromethylthienobenzoxazole dioxide; thienobenzoxazole dioxide dihydro methyl; fluoronitrobenzothiazole; chloronitrobenzothiazole fluoride substitution; nitrobenzothiazole fluoro; benzothiazole nitro fluoro. We’ll tell you more about this compound (cas:2407-11-6).

6-Azidobenzothiazole and its 2-Me and 2-(methylthio) derivatives, prepared from the corresponding amines by diazotization and reaction with NaN3, gave the thiazolo[4,5-g]benzoxazoles I (R = H, Me, SH) (50, 42 and 20%, resp.) on thermolysis (120°, 1.5 h) in a polyphosphoric acid-HOAc mixture Under similar conditions 6-azido-2,3-dihydrobenzo[b]thiophene 1,1-dioxide gave 11% II. 2-Fluoro-6-nitrobenzothiazole was prepared in almost quant. yield by reaction of the chloro analog with F- in MeCN containing 18-crown-6.

There is still a lot of research devoted to this compound(SMILES:O=[N+](C1=CC=C2N=C(Cl)SC2=C1)[O-])HPLC of Formula: 2407-11-6, and with the development of science, more effects of this compound(2407-11-6) can be discovered.

Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI