39964-85-7

Usage

Uses

Used in Pharmaceutical Research:
2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine is used as a research compound for exploring its potential pharmacological properties. Its unique molecular structure may contribute to the development of new drugs or therapeutic agents.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, 2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine is used as a starting material or intermediate in the synthesis of more complex organic molecules. Its complex structure provides opportunities for further chemical reactions and modifications.
Used in Chemical Synthesis Studies:
2,2-dimethoxy-N-<(3',4',5'-trimethoxyphenyl)methylene>ethylamine is utilized in chemical synthesis studies to understand the reactivity and behavior of its functional groups and substituents. This knowledge can be applied to optimize synthetic routes and develop new synthetic methodologies.

Upstream product

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

Downstream Products

• 54879-83-3 N-(2'',2''-dimethoxyethyl)-3',4',5'-trimethoxyphenylmethylamine 
• 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 

Relevant academic research and scientific papers

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,

Synthesis of Indenoisoquinoliniums and Methods of Use

Substituted indenoisoquinolinium compounds, and pharmaceutical formulations of substituted indenoisoquinolinium compounds are described. Also described are processes for preparing substituted indenoisoquinolinium compounds. Also described are methods for

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)