38825-43-3

Upstream product

• 105-36-2 ethyl bromoacetate 
• 1424-14-2 dibenzyl thiourea 
• 622-78-6 Benzyl isothiocyanate 
• 100-46-9 benzylamine 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 17945-00-5 3-benzyl-2-benzylimino-5-{4-[bis-(2-chloro-ethyl)-amino]-phenylimino}-thiazolidin-4-one 
• 17944-97-7 3-benzyl-2-benzylimino-5-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-thiazolidin-4-one 
• 23155-46-6 3-benzyl-2-benzylimino-thiazolidine-4,5-dione 5-[(4-nitro-phenyl)-hydrazone] 
• 58953-99-4 3-benzyl-2-benzylimino-5-(bis-methylsulfanyl-methylene)-thiazolidin-4-one 
• 38825-59-1 3-benzyl-2-benzylimino-1,1-dioxo-1λ⁶-thiazolidin-4-one 
• 56383-54-1 3-benzyl-2-benzylimino-6-methylsulfanyl-2,3-dihydro-[1,3]thiazin-4-one 

Relevant academic research and scientific papers

Electrogenerated base-promoted synthesis and antimicrobial activity of 2-imino-1,3-thiazolidin-4-one derivatives

Electrogenerated cyanomethylanions obtained by reduction of dry acetonitrile at a steel grid cathode were used to promote the addition of ethyl bromoacetate to thiourea derivatives. The reaction yields the corresponding 2-imino-1,3-thiazolidin-4-one. The

Facile and regioselective synthesis of thiazolidin-4-one derivatives catalyzed by basic ionic liquid [bmim]OH under ultrasonic irradiation

2-Iminothiazolidin-4-one derivatives were synthesized regioselectively in good to high yields by condensation of N,N-disubstituted thioureas and ethyl chloroacetate in the presence of basic ionic liquid [bmim]OH as a catalyst under conventional and ultrasonic irradiation conditions. Under ultrasonic irradiation, the reaction furnished the desired 2-iminothiazolidinones in higher yields (76-87%) and lower reaction times (30-55 min).