114651-98-8

Basic information

• Product Name: (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylaldehyde
• Synonyms: (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylaldehyde
• CAS NO: 114651-98-8
• Molecular Weight: 298.339
• Mol File: 114651-98-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylaldehyde(114651-98-8)
• EPA Substance Registry System: (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylaldehyde(114651-98-8)

Safety Data

• Hazardous Substances Data: 114651-98-8(Hazardous Substances Data)

Upstream product

• 114651-97-7 2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)-(E)-propenol 
• 87101-68-6 (E)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)-acrylic acid methyl ester 
• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 123-11-5 4-methoxy-benzaldehyde 
• 37629-77-9 (Z)-2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylonitrile 

Downstream Products

• 23365-39-1 2-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)-1,6,7,8,9,9a-hexahydro-4H-quinolizin-4-one 
• 114652-01-6 7-(3,4-dimethoxyphenyl)-8-(4-methoxyphenyl)-(E)-5,7-octadienamide 
• 114652-05-0 isojulandine 
• 114652-03-8 7-(3,4-dimethoxyphenyl)-8-(4-methoxyphenyl)-(E)-5,7-octadienylamine 
• 1346463-43-1 4-(3,4-dimethoxyphenyl)-5-(4-methoxyphenyl)penta-(2E,4Z)-dienoic acid 
• 1346463-56-6 4-(3,4-dimethoxyphenyl)-5-(4-methoxyphenyl)penta-(2E,4Z)-dienoyl azide 

Relevant articles and documents

PHENANTHROINDOLIZIDINE AND PHENANTHROQUINOLIZIDINE ALKALOID HAVING A HYDROXYL GROUP ON THE PHENANTHRENE RING THEREOF, PREPARATION METHOD AND USE THEREOF

A phenanthroindolizidine and phenanthroquinolizidine alkaloid having a hydroxyl group on the phenanthrene ring thereof was synthesized, which exhibits potent activity as an anticancer agent against, such as breast cancer, lung cancer, and prostate cancer.

Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: Mechanistic studies

The thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates 1, generated in situ from the corresponding azides, was investigated using iodine as a catalyst. Diphenylpyridinones 2, phenylnaphthalenes 3, and indenes 4 were produced via intramolecular ring closure. The nature of the substituents on the phenyl rings was found to be crucial to the distribution of cyclized products 2 - 4. The mechanism of the reaction is also discussed.