39964-85-7

Basic information

• Product Name: 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine
• Synonyms: 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine
• CAS NO: 39964-85-7
• Molecular Weight: 283.324
• Mol File: 39964-85-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine(39964-85-7)
• EPA Substance Registry System: 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine(39964-85-7)

Safety Data

• Hazardous Substances Data: 39964-85-7(Hazardous Substances Data)

Usage

General Description

2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine is a chemical compound with a complex structure, consisting of a central amine group linked to a dimethoxyethyl chain and a substituted phenyl moiety. The compound is characterized by its unique and intricate molecular architecture, with multiple substituents and functional groups. It may have potential applications in pharmaceutical research, due to its structural features and potential pharmacological properties. Additionally, its complex structure may also make it of interest for synthetic chemistry and chemical synthesis studies. However, further research and analysis are needed to fully understand its properties and potential uses.

Upstream product

• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 22483-09-6 2,2-dimethoxyethylamine 

Downstream Products

• 148492-83-5 ethyl 2-benzoyl-1-cyano-8-ethoxycarbonyl-5,6,7-trimethoxy-1,2-dihydroisoquinoline-1-ethanoate 
• 148492-78-8 ethyl 2-benzoyl-1-cyano-5,6,7-trimethoxy-1-methyl-1,2-dihydroisoquinoline-8-carboxylate 
• 148492-77-7 ethyl 2-benzoyl-1-cyano-5,6,7-trimethoxy-1,2-dihydroisoquinoline-8-carboxylate 
• 39964-89-1 N-(2'',2''-dimethoxyethyl)-4-methyl-N-(3''',4''',5'''-trimethoxyphenylmethyl)benzene sulfonamide 
• 36982-71-5 5,6,7-trimethoxyisoquinoline 
• 54879-83-3 N-(2'',2''-dimethoxyethyl)-3',4',5'-trimethoxyphenylmethylamine 

Relevant articles and documents

Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis

Several norindenoisoquinolines substituted with methoxy or methylenedioxy groups have been prepared and their anticancer properties evaluated in cancer cell cultures and in topoisomerase I inhibition assays. 2,3-Dimethoxy-8,9- methylenedioxy-11H-indeno[1,

Studies Directed Towards Total Syntheses of the Tropoloisoquinoline Alkaloids Grandirubrine and Imerubrine. I. Preparation of Two 4,5,6-Trimethoxycyclopentisoquinolin-7-ones and Their Response to Robinson Annulation Conditions

In connection with efforts to develop total syntheses of the tropoloisoquinoline alkaloids grandirubrine (1) and imerubrine (2), preparations of tricyclic ketone (8) and the related ethoxycarbonyl system (47) are described.Of the various approaches to (8)