1,2,4-dithiazolidines; synthesis, antibacterial and antifungal activity was written by Deohate, Pradip P.;Berad, B. N.. And the article was included in Chemistry: An Indian Journal in 2004.Related Products of 57179-35-8 This article mentions the following:
3,5-Diphenylimino-4-alkylbenzylidene amidino-1,2,4-dithiazolidines, e.g., I, have been obtained by the basification of their hydrochlorides, which were prepared by efficient method of interaction of N-phenyl-S-chloro isothiocarbamoyl chloride and 1-(substituted) alkylbenzylidene amidino-3-Ph thiocarbamides. The latter were synthesized by the condensation of 1-amidino-3-Ph thiocarbamide and different aliphatic and aromatic aldehydes. 3,5-Diphenylimino-4-alkylbenzylidene amidino-1,2,4-dithiazolidines underwent acylation to afford monoacetyl derivatives, and on reaction with sodium nitrite in acidic medium afforded mononitroso derivatives The title compounds were assayed for their antibacterial and antifungal activity against gram pos. as well as gram neg. microorganisms. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8Related Products of 57179-35-8).
3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Related Products of 57179-35-8
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem