676596-89-7

Upstream product

• 676597-02-7 4-(tert-butyl-dimethyl-silanyloxy)-3-(2-fluoro-ethyl)-benzaldehyde 
• 34841-06-0 3-bromo-4-methoxybenzylaldehyde 
• 103929-84-6 [3,5-di(tert-butyldimethylsilanyloxy)phenyl]methanol 
• 676597-01-6 toluene-4-sulfonic acid 2-(5-formyl-2-methoxymethoxy-phenyl)-ethyl ester 
• 676596-99-9 2-(5-hydroxymethyl-2-methoxymethoxy-phenyl)-ethanol 
• 676597-59-4 3-(2-fluoro-ethyl)-4-methoxymethoxy-benzaldehyde 
• 676597-00-5 3-(2-hydroxy-ethyl)-4-methoxymethoxy-benzaldehyde 
• 162269-90-1 3-bromo-4-(methoxymethoxy)benzaldehyde 
• 158139-69-6 5-(bromomethyl)-1,3-bis(tert-butyldimethylsilyloxy)-benzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 2973-78-6 3-bromo-4-hydroxybenzylaldehyde 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 

Relevant academic research and scientific papers

Syntheses and radical scavenging activities of resveratrol derivatives

Nine new resveratrol derivatives, having bromo, iodo, and fluoroethyl groups, were designed and synthesized. All compounds having free phenol groups showed good free radical scavenging activity. Among them, 2-bromoresveratrol 19 has a similar free radical scavenging activity to (+)-catechin.