28996-11-4

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 72425-41-3 2-Mercapto-5-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-thiazol-4-one; compound with triethyl-amine 
• 74-88-4 methyl iodide 
• 5462-97-5 5-(4-methoxybenzylidene)-2-thioxo-4-thiazolidinone 
• 77-78-1 dimethyl sulfate 
• 186581-53-3 diazomethane 

Downstream Products

• 55111-58-5 5-(4-Methoxyphenylmethylene)-4-oxo-2-piperidino-2-thiazoline 
• 36937-45-8 5-(4-Methoxyphenylmethylene)-2-morpholino-2-thiazolin-4-one 
• 76979-40-3 5-(4-Methoxyphenylmethylene)-2-(4-methylphenylimino)-4-thiazolidinone 
• 76979-41-4 5-(4-Methoxyphenylmethylene)-2-(4-methoxyphenylimino)-4-thiazolidinone 
• 76979-45-8 5-(4-Methoxyphenylmethylene)-2-(4-methylphenylmethylimino)-4-thiazolidinone 
• 76979-51-6 5-(4-Methoxyphenylmethylene)-2-(phenylmethylimino)-3-methyl-4-thiazolidinone 
• 76979-43-6 5-(4-Methoxyphenylmethylene)-2-(phenylmethylimino)-4-thiazolidinone 
• 76979-47-0 5-(4-Methoxyphenylmethylene)-2-(4-methoxyphenylmethylimino)-4-thiazolidinone 
• 36946-72-2 5-(4-Methoxyphenylmethylene)-2-imino-4-thiazolidinone 
• 6320-51-0 5-(4-methoxybenzylidene)thiazolidine-2,4-dione 
• 99819-31-5 2-Allylamino-5-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-thiazol-4-one 

Relevant academic research and scientific papers

Combination of 4-anilinoquinazoline and rhodanine as novel epidermal growth factor receptor tyrosine kinase inhibitors

Abstract A type of novel rhodanine-based 4-anilinoquinazoline, which designed the combination between quinazoline as the backbone and various substituted biological rhodanine groups as the side chain, have been synthesized, and their antiproliferative act

REACTIVITY AND TATUMERISM OF AZOLIDINES. XXXI.* KINETICS OF THE METHYLATION OF 5-ARYLIDENERHODANINES

The kinetics of the methylation of the triethylammonium salt of 5-arylidenerhodanines in dimethylformamide were investigated.The rate constants were determined for methylation at each center of the ambident anion of the substrate.A correlation was obtained between the reaction rate constants and the constants of the substituents in the arylidene group.Proposals are made about the transmission of the effect of the substituent to the ambident reaction center.