491610-76-5

Upstream product

• 491610-74-3 benzyl 3-(2,4-dibenzyloxyphenyl)propionate 
• 5631-68-5 3-(2,4-Dihydroxyphenyl)propionic Acid 
• 98-59-9 p-toluenesulfonyl chloride 
• 491610-75-4 3-(2',4'-di(benzyloxy)phenyl)propanol 

Downstream Products

• 491610-80-1 1,11-bis(5-cyano-2,4-dibenzyloxyphenyl)-4,8-dioxaundecane 
• 491610-79-8 1,11-bis(2,4-dibenzyloxy-5-formylphenyl)-4,8-dioxaundecane 
• 491610-78-7 1,11-bis(2,4-dibenzyloxyphenyl)-4,8-dioxaundecane 
• 491610-81-2 1,11-bis(5-cyano-2,4-dihydroxyphenyl)-4,8-dioxaundecane 
• 491610-77-6 1-(3-bromopropyl)-2,4-dibenzyloxybenzene 
• 115692-62-1 1-Allyl-2,4-bis-benzyloxy-benzene 

Relevant academic research and scientific papers

Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin

Free radicals and reactive oxygen species have the potential to damage a wide variety of organic molecules, typically by oxidizing certain moieties. These damaging species can, for example, be produced by an organism as a by-product of cellular respiratio

Desferrithiocin analogue based hexacoordinate iron(III) chelators

Traditional thinking has been that hexacoordinate Fe(III) ligands are more effective at preventing iron's interactions with reactive oxygen species, most particularly the Fe(II)-mediated reduction of hydrogen peroxide to the hydroxyl radical (i.e., Fenton