141070-41-9

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 104-87-0 4-methyl-benzaldehyde 
• 79010-36-9 2-Acetyl-4-propionylphenol 

Downstream Products

• 141070-43-1 3-Hydroxy-6-propionyl-2-p-tolyl-chromen-4-one 
• 141070-59-9 2-(3-Benzyloxy-4-oxo-2-p-tolyl-4H-chromen-6-yl)-propionic acid methyl ester 
• 141070-67-9 2-(3-Benzyloxy-4-oxo-2-p-tolyl-4H-chromen-6-yl)-propionic acid 
• 141070-52-2 3-Benzyloxy-2-(4-chloro-phenyl)-6-propionyl-chromen-4-one 
• 141070-51-1 3-Benzyloxy-6-propionyl-2-p-tolyl-chromen-4-one 
• 141070-55-5 2-(3-Methoxy-4-oxo-2-p-tolyl-4H-chromen-6-yl)-propionic acid methyl ester 
• 141070-63-5 2-(3-Methoxy-4-oxo-2-p-tolyl-4H-chromen-6-yl)-propionic acid 
• 141070-47-5 3-Methoxy-6-propionyl-2-p-tolyl-chromen-4-one 

Relevant academic research and scientific papers

Synthesis and anticomplementary activity of 2-(2-aryl-3-alkoxychromon-6-yl)propanoic acids

The title compounds have been synthesized from the corresponding 2-aryl-3-alkoxy-6-propionylchromones by 1,2-migration of chromone ring using hypervalent iodine reagents.Seven selected compounds have been found to inhibit the in vitro immunohaemolysis of