89946-15-6

Basic information

• Product Name: Benzene, 5-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2,3-trimethoxy-, (E)-
• CAS NO: 89946-15-6
• Molecular Formula: C19H22O5
• Molecular Weight: 330.381
• Mol File: 89946-15-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, 5-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2,3-trimethoxy-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 5-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2,3-trimethoxy-, (E)-(89946-15-6)
• EPA Substance Registry System: Benzene, 5-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2,3-trimethoxy-, (E)-(89946-15-6)

Safety Data

• Hazardous Substances Data: 89946-15-6(Hazardous Substances Data)

Upstream product

• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 667458-79-9 3,5-dimethoxybenzyl 3,5-bis(trifluoromethyl)phenyl sulfone 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 61240-20-8 triphenyl-(3,4,5-trimethoxybenzyl)phosphonium bromide 
• 25245-29-8 5-iodo-1,2,3-trimethoxybenzene 
• 40243-87-6 3,5-dimethoxystyrene 
• 108957-75-1 diethyl 3,5-dimethoxybenzylphosphonate 
• 24131-30-4 (3,5-dimethoxybenzyl)triphenylphosphonium bromide 
• 397333-50-5 (3,5-dimethoxy-benzyl)phosphonic acid dimethyl ester 
• 877-88-3 3,5-dimethoxybenzyl bromide 
• 186581-53-3 diazomethane 
• 35154-48-4 3,3',4',5,5'-pentahydroxystilbene 
• 134029-74-6 [(3,4,5-trimethoxyphenyl)methyl]phosphoric acid diethyl ester 

Downstream Products

• 35154-48-4 3,3',4',5,5'-pentahydroxystilbene 
• 52961-91-8 3.3'.4.5.5'-Pentamethoxybibenzyl 

Relevant articles and documents

Anticancer Evaluation of 3,4,5,4'-trans-tetramethoxystilbene (DMU-212) and Its Analogs Against an Extensive Panel of Human Tumor Cell Lines

DMU-212, a methoxylated resveratrol analog, has significant anticancer activity, and selectively targets tumor cells. A library of E-diarylstilbenes structurally related to DMU-212 has been synthesized and evaluated for anticancer activity against a large

Synthesis of substituted styrenes and stilbenes mediated by palladium on zirconia

Palladium on zirconia has been found to be an effective catalyst for the synthesis of various substituted styrenes and stilbenes, including biologically active natural products, by reaction of aryl halides with olefins.

Stilbene-based anticancer agents: Resveratrol analogues active toward HL60 leukemic cells with a non-specific phase mechanism

Several stilbenes, related to known resveratrol, have been synthesized and tested for their anticancer effect on HL60 leukemia cell line, taking particular care of the cell cycle analysis. The most potent compound was the known (Z)-3,4′,5-trimethoxystilbe