(3aR,7aR)-4-(benzo[d]isothiazol-3-yl)octahydrospiro[isoindole-2,1-piperazin]-2-ium4-methylbenzenesulfonate. CAS:1907680-83-4

The isoindole portion of the molecule is a bicyclic structure that contains a nitrogen-containing heterocycle. The addition of a benzo[d]isothiazolyl group at the 4-position of the isoindole moiety further enhances the molecule's complexity and potential for biological activity. Benzo[d]isothiazoles are known for their antimicrobial, antifungal, and antiviral properties, which may contribute to the overall biological profile of the compound. The piperazine ring, a six-membered heterocycle containing two nitrogen atoms, adds flexibility to the molecule and can participate in various types of chemical reactions. Piperazine derivatives are often found in pharmaceuticals due to their pharmacological properties, such as antitussive, antihistamine, and antidepressant activities. The 4-methylbenzenesulfonate counterion, attached to the piperazine nitrogen, helps to balance the charge of the positively charged ammonium ion. Sulfonates are commonly used as counterions in organic salts because they are relatively inert and soluble in water, which facilitates the handling and administration of the compound. Given its complex structure and the presence of various functional groups, this molecule is likely to exhibit a range of biological activities. It could potentially be used as a therapeutic agent or a starting point for further drug development. The synthesis of such a compound would require a carefully planned sequence of organic reactions, involving the formation of the spirocyclic core, the introduction of the substituents, and finally, the salt formation with the sulfonate counterion. The molecule's potential applications would depend on its biological activity, which would need to be evaluated through extensive research and clinical trials.