15109-37-2

Usage

Uses

Used in Organic Synthesis:
(4,7-DIMETHOXY-1H-INDOL-3-YL)-ACETONITRILE is used as a building block for the synthesis of more complex organic molecules. Its unique structure allows for a variety of chemical reactions, making it a versatile compound in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4,7-DIMETHOXY-1H-INDOL-3-YL)-ACETONITRILE is used as an intermediate in the development of new drugs. Its specific properties may contribute to the creation of novel therapeutic agents with potential applications in various medical conditions.
Used as a Research Reagent:
(4,7-DIMETHOXY-1H-INDOL-3-YL)-ACETONITRILE is also utilized as a research reagent in chemical and biological studies. Its distinctive structure and functional groups make it a valuable tool for understanding various chemical and biological processes, potentially leading to new discoveries and advancements in these fields.

InChI:InChI=1/C12H12N2O2/c1-15-9-3-4-10(16-2)12-11(9)8(5-6-13)7-14-12/h3-4,7,14H,5H2,1-2H3

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 23876-39-3 4,7-dimethoxylindole 
• 92033-00-6 1-(4,7-dimethoxy-1H-indol-3-yl)-N,N-dimethylmethanamine 

Downstream Products

• 91557-43-6 2-(4,7-dimethoxy-1H-indol-3-yl)ethylamine 
• 220034-71-9 tert-butyl (2-{4,7-dimethoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl}ethyl)carbamate 
• 220034-57-1 tert-butyl (2-{1-[(4-methylphenyl)sulfonyl]-4,7-dioxo-4,7-dihydro-1H-indol-3-yl}ethyl)carbamate 
• 892112-74-2 tert-butyl (2-{1-(3-hydroxy-1-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-7-[(4-methylphenyl)sulfonyl]-4,8-dioxo-1,4,7,8-tetrahydro-pyrrolo[3,2-f]indazol-5-yl}ethyl)carbamate 
• 892113-17-6 tert-butyl (2-{1-(3-hydroxy-1-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-5-[(4-methylphenyl)sulfonyl]-4,8-dioxo-1,4,5,8-tetrahydro-pyrrolo[2,3-f]indazol-7-yl}ethyl)carbamate 
• 892113-84-7 7-(3-hydroxy-1-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-5-(toluene-4-sulfonyl)-2,3,5,9-tetrahydro-1,5,8,9-tetraaza-cyclopenta[e]acenaphthylen-6-one 
• 892113-50-7 9-(3-hydroxy-1-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-5-[(4-methylphenyl)sulfonyl]-2,3,5,7-tetrahydro-6H-pyrazolo[3,4-h]pyrrolo[4,3,2-de]quinolin-6-one 
• 892113-24-5 5-(toluene-4-sulfonyl)-2,3,5,7-tetrahydro-1,5,7,8-tetraaza-cyclopenta[e]acenaphthylen-6-one 
• 892113-57-4 5-(toluene-4-sulfonyl)-2,3,5,9-tetrahydro-1,5,8,9-tetraaza-cyclopenta[e]acenaphthylen-6-one 
• 892113-63-2 9-methyl-5-[(4-methylphenyl)sulfonyl]-2,3,5,9-tetrahydro-6H-pyrazolo[4,3-h]pyrrolo[4,3,2-de]quinolin-6-one 
• 892113-31-4 7-methyl-5-(toluene-4-sulfonyl)-2,3,5,7-tetrahydro-1,5,7,8-tetraaza-cyclopenta[e]acenaphthylen-6-one 

Relevant academic research and scientific papers

Synthesis and antitumor characterization of pyrazolic analogues of the marine pyrroloquinoline alkaloids: Wakayin and tsitsikammamines

A series of aza analogues of the marine alkaloids wakayin and tsitsikammamines A and B have been synthesized. The strategy used was based on [3 + 2] cycloaddition reactions involving 3-ethylamine-indole-4,7-dione and different diazo reagents. All the comp