93515-32-3

Upstream product

• 81154-19-0 (Z)-5-(4-chlorobenzylidene)-2-sulfanylidenethiazolidin-4-one 

Downstream Products

• 1353992-38-7 5-(4-chlorobenzylidene)-2-phenyl-3-(4-methyphenyl)-4-thiazolidinone 
• 1353992-39-8 5-(4-chlorobenzylidene)-3-(4-chlorophenyl)-2-(4-dimethylaminophenyl)-4-thiazolidinone 
• 74942-64-6 5-(4-chloro-benzylidene)-thiazolidine-2,4-dione 
• 1352309-07-9 (Z)-2-amino-4[(4-chlorophenylmethylene)-2-trichloromethyl]-1,3-oxathiolan-5-one 
• 1352309-15-9 (Z)-5-[4-(chlorophenylmethylene)-2-ethoxy-2-(trichloromethyl)]thiazolidin-4-one 
• 1352309-23-9 (Z)-5-[4-(chlorophenylmethylene)-2-methoxy-2-(trichloromethyl)]-thiazolidin-4-one 
• 1352309-31-9 (Z)-5-[4-(chorophenylmethylene)-2-propoxy-2-(trichloromethyl)]-thiazolidin-4-one 
• 93515-61-8 4-[1-(4-Chloro-phenyl)-meth-(Z)-ylidene]-2-methylene-[1,3]oxathiolan-5-one 

Relevant academic research and scientific papers

An efficient method for the transformation of 5-ylidenerhodanines into 2,3,5-trisubstituted-4-thiazolidinones

The use of 3-substituted-2-mercaptoacrylic acids, synthesized via hydrolysis of 5-ylidenerhodanines for the preparation of 2,3,5-trisubstituted-4- thiazolidinones via a new variant of the one-pot, three-component reaction has been studied.