1326634-95-0

Basic information

• Product Name: trans,trans,trans-1-(3,5-dihydroxyphenyl)-6-(4-hydroxyphenyl)-1,3,5-hexatriene
• CAS NO: 1326634-95-0
• Molecular Weight: 280.323
• Mol File: 1326634-95-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: trans,trans,trans-1-(3,5-dihydroxyphenyl)-6-(4-hydroxyphenyl)-1,3,5-hexatriene(CAS DataBase Reference)
• NIST Chemistry Reference: trans,trans,trans-1-(3,5-dihydroxyphenyl)-6-(4-hydroxyphenyl)-1,3,5-hexatriene(1326634-95-0)
• EPA Substance Registry System: trans,trans,trans-1-(3,5-dihydroxyphenyl)-6-(4-hydroxyphenyl)-1,3,5-hexatriene(1326634-95-0)

Safety Data

• Hazardous Substances Data: 1326634-95-0(Hazardous Substances Data)

Upstream product

• 832-01-9 methyl p-methoxycinnamate 
• 147663-61-4 3-(3,5-dimethoxyphenyl)prop-2-en-1-ol 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 53484-50-7 p-methoxycinnamyl alcohol 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 16034-99-4 1-(2-bromopropenyl)-4-methoxybenzene 
• 125187-46-4 3,5-dimethoxycinnamaldehyde 
• 879583-48-9 C₁₄H₂₁O₄P 
• 76104-60-4 methyl 3-(3,5-dimethoxyphenyl)acrylate 

Relevant articles and documents

Finding more active antioxidants and cancer chemoprevention agents by elongating the conjugated links of resveratrol

Resveratrol is the subject of intense research as a natural antioxidant and cancer chemopreventive agent. There has been a great deal of interest and excitement in understanding its action mechanism and developing analogs with antioxidant and cancer chemoprevention activities superior to that of the parent compound in the past decade. This work delineates that elongation of the conjugated links is an important strategy to improve the antioxidant activity of resveratrol analogs, including hydrogen atom- or electron-donating ability in homogeneous solutions and antihemolysis activity in heterogeneous media. More importantly, C3, a triene bearing 4,4′-dihydroxy groups, surfaced as an important lead compound displaying remarkably increased antioxidant, cytotoxic, and apoptosis-inducing activities compared with resveratrol.