54922-76-8

Basic information

• Product Name: (E)-1-(benzyloxy)-4-(3,5-dimethoxystyryl)-2-methoxybenzene
• Synonyms: (E)-1-(benzyloxy)-4-(3,5-dimethoxystyryl)-2-methoxybenzene
• CAS NO: 54922-76-8
• Molecular Weight: 376.452
• Mol File: 54922-76-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-1-(benzyloxy)-4-(3,5-dimethoxystyryl)-2-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(benzyloxy)-4-(3,5-dimethoxystyryl)-2-methoxybenzene(54922-76-8)
• EPA Substance Registry System: (E)-1-(benzyloxy)-4-(3,5-dimethoxystyryl)-2-methoxybenzene(54922-76-8)

Safety Data

• Hazardous Substances Data: 54922-76-8(Hazardous Substances Data)

Upstream product

• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 877-88-3 3,5-dimethoxybenzyl bromide 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 498-00-0 4-hydroxymethyl-2-methoxyphenol 
• 33693-48-0 4-benzyloxy-3-methoxybenzyl alcohol 
• 100-39-0 benzyl bromide 
• 72724-00-6 1-(benzyloxy)-4-(bromomethyl)-2-methoxybenzene 
• 24131-30-4 (3,5-dimethoxybenzyl)triphenylphosphonium bromide 
• 108957-75-1 diethyl 3,5-dimethoxybenzylphosphonate 

Downstream Products

• 108957-72-8 (trans)-4-[2-(3,5-dimethoxyphenyl)ethenyl]-2-methoxyphenol 

Relevant articles and documents

Prevention of Marine Biofouling Using the Natural Allelopathic Compound Batatasin-III and Synthetic Analogues

The current study reports the first comprehensive evaluation of a class of allelopathic terrestrial natural products as antifoulants in a marine setting. To investigate the antifouling potential of the natural dihydrostilbene scaffold, a library of 22 syn

Syntheses of resveratrol and its hydroxylated derivatives as radical scavenger and tyrosinase inhibitor

Eight hydroxylated stilbene derivatives including resveratrol, desoxyrhapontigenin and piceatannol as potential radical scavenger and tyrosinase inhibitor are synthesized using optimized Wittig-Horner reaction for excellent trans-selectivity in good yields. Antioxidant activity was tested against ABTS radical and tyrosinase inhibitory activity was performed with L-tyrosine as the substrate based on previous procedure with some modification. In general, catecholic stilbenes showed stronger activity against ABTS radical and resorcinolic moiety showed stronger tyrosinase inhibitory activity. Synthetic piceatannol which containing both catecholic and resorcinolic moieties showed the strongest activity in both as ABTS radical scavenger and tyrosinase inhibitor with IC50 values of 4.1 and 8.6 μM, respectively.