135082-73-4

Usage

Structure

2,5-Cyclohexadiene-1,4-dione core with (3-methoxyphenyl)amino and methyl substituents

Derivative

2,5-cyclohexadiene-1,4-dione

Substituents

3-methoxyphenylamino group and a methyl group

Potential uses

Pharmaceutical and organic synthesis

Possible properties

Pharmacological properties or biological activity

Presence

Phenylamino group

Determination of properties

Further research and testing required

Upstream product

• 536-90-3 m-Anisidine 
• 553-97-9 2-Methyl-1,4-benzoquinone 

Downstream Products

• 96861-91-5 pyrayaquinone B 

Relevant academic research and scientific papers

Indoloquinones, part 8.1 palladium(II)-catalyzed total synthesis of murrayaquinone A, koeniginequinone A, and koeniginequinone B

Regioselective addition of the appropriate arylamines to 2-methyl-1,4-benzoquinone followed by a palladium(II)-catalyzed oxidative cyclization opens up an efficient route to the naturally occurring 3-methylcarbazole-1,4-quinone alkaloids murrayaquinone A, koeniginequinone A, and koeniginequinone B.

Synthesis of carbazoloquinone derivatives and their antileukemic activity via modulating cellular reactive oxygen species

Carbazoloquinone alkaloids are of great interest as privileged structures for anticancer drug molecules. The purpose of this study was to investigate the structure-activity relationships of carbazoloquinone derivatives as anticancer agents. A series of ca