Castellanos, Maria Luisa; Llinas, Montserrat; Bruix, Marta; De Mendoza, Javier; Martin, M. Rosario published the artcile< NN'-linked biazoles. Part 4. Nucleophilic substitution in quaternary salts of NN'-linked biazoles and related systems>, SDS of cas: 17827-61-1, the main research area is nucleophile substitution biazolyl cation azolylpyridinium; pyridinium azolyl substitution nucleophile.
Some di- and monocationic N,N’-linked biazoles and quaternized 1-(N-azolyl)pyridinium ions were prepared and their reactions with nucleophiles were studied. Although the pyrrolyl nucleus is a poor leaving group in these reactions, in other cases nucleophilic attack readily occurs at an azolyl C, with subsequent elimination of the N substituent. E.g., reaction of dication I with NaCN in H2O at room temperature for 18 h gave 80% 2-cyano-1-methylbenzimidazole and 7% 1-methylbenzimidazol-2-one.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) published new progress about Hydrolysis kinetics. 17827-61-1 belongs to class pyrazoles-derivatives, and the molecular formula is C6H8N2O2, SDS of cas: 17827-61-1.
Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics