422566-49-2

Basic information

• Product Name: 6,7-dimethoxy-1-[1-(3,4-dimethoxyphenyl)-2-(2-methoxymethoxy-4,5-methylenedioxyphenyl)-2-oxoethyl]isoquinoline
• Synonyms: 6,7-dimethoxy-1-[1-(3,4-dimethoxyphenyl)-2-(2-methoxymethoxy-4,5-methylenedioxyphenyl)-2-oxoethyl]isoquinoline
• CAS NO: 422566-49-2
• Molecular Weight: 547.562
• Mol File: 422566-49-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6,7-dimethoxy-1-[1-(3,4-dimethoxyphenyl)-2-(2-methoxymethoxy-4,5-methylenedioxyphenyl)-2-oxoethyl]isoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6,7-dimethoxy-1-[1-(3,4-dimethoxyphenyl)-2-(2-methoxymethoxy-4,5-methylenedioxyphenyl)-2-oxoethyl]isoquinoline(422566-49-2)
• EPA Substance Registry System: 6,7-dimethoxy-1-[1-(3,4-dimethoxyphenyl)-2-(2-methoxymethoxy-4,5-methylenedioxyphenyl)-2-oxoethyl]isoquinoline(422566-49-2)

Safety Data

• Hazardous Substances Data: 422566-49-2(Hazardous Substances Data)

Upstream product

• 82146-04-1 methyl 6-hydroxybenzo[d][1,3]dioxole-5-carboxylate 
• 4720-68-7 4,5-methylenedioxy-2-hydroxybenzaldehyde 
• 58-74-2 Papaverine 
• 422566-45-8 6-methoxymethoxy-benzo[1,3]dioxole-5-carboxylic acid methyl ester 

Relevant articles and documents

Synthesis and structure-activity relationship study of lamellarin derivatives

Ten derivatives (3-12) of marine alkaloid lamellarin D (1) were synthesized and evaluated for cytotoxicity against a HeLa cell line in an effort to examine their structure-activity relationships. It appeared that the hydroxyl groups at positions C-8 and C-20 of 1 were important structural requirements for cytotoxic activity, while the hydroxyl group at C-14 and the two methoxy groups at C-13 and C-21 were not necessary for the activity.