3698-06-4

Upstream product

• 141-84-4 2-thioxo-4-thiazolidinone 
• 108-94-1 cyclohexanone 

Downstream Products

• 86199-39-5 5-cyclohexyLiDene-thiazolidine-2,4-dione 
• 1236049-29-8 N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-cyclohexylidene-2-thioxo-4-thiazolidinone 
• 28996-31-8 3-(4-bromo-anilinomethyl)-5-cyclohexylidene-2-thioxo-thiazolidin-4-one 
• 29004-62-4 5-cyclohexylidene-3-(4-fluoro-anilinomethyl)-2-thioxo-thiazolidin-4-one 
• 29004-24-8 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-(2-methyl-2-aza-propane-1,3-diyl)-bis-thiazolidin-4-one 
• 29004-61-3 5-cyclohexylidene-3-(3-methyl-anilinomethyl)-2-thioxo-thiazolidin-4-one 
• 28996-33-0 3-(2-chloro-anilinomethyl)-5-cyclohexylidene-2-thioxo-thiazolidin-4-one 
• 28996-32-9 3-(3-chloro-anilinomethyl)-5-cyclohexylidene-2-thioxo-thiazolidin-4-one 
• 29004-60-2 3-anilinomethyl-5-cyclohexylidene-2-thioxo-thiazolidin-4-one 
• 29004-28-2 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-(2-butyl-2-aza-propane-1,3-diyl)-bis-thiazolidin-4-one 
• 29004-27-1 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-(2-isopropyl-2-aza-propane-1,3-diyl)-bis-thiazolidin-4-one 
• 29004-31-7 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-[2-(2-hydroxy-ethyl)-2-aza-propane-1,3-diyl]-bis-thiazolidin-4-one 
• 29004-25-9 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-(2-ethyl-2-aza-propane-1,3-diyl)-bis-thiazolidin-4-one 
• 29004-29-3 5,5'-dicyclohexylidene-2,2'-dithioxo-3,3'-(2-isobutyl-2-aza-propane-1,3-diyl)-bis-thiazolidin-4-one 

Relevant academic research and scientific papers

Facile and convenient synthesis of 5-arylalkylidenerhodanines by electrocatalytic crossed aldol condensation

An electrochemically induced catalytic crossed Aldol condensation of one equivalent of rhodanine with various aromatic aldehydes and ketones in ethanol in an undivided cell in the presence of sodium bromide as an electrolyte results in the formation of th

Synthesis and antimicrobial activity of some new N-glycosides of 2-thioxo-4-thiazolidinone derivatives

5-Arylidene-2-thioxo-4-thiazolidinones 3a-f react with each of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl and α-d-galactopyranosyl bromides 4a,b in acetone in the presence of aqueous potassium hydroxide at room temperature to afford N-(2,3,4,6-tetra-O-acet