55868-85-4

Upstream product

• 82-45-1 1-amino-9,10-anthracenedione 
• 98-59-9 p-toluenesulfonyl chloride 
• 82-44-0 1-chloroanthracene-9,10-dione 
• 70-55-3 toluene-4-sulfonamide 
• 941-55-9 4-toluenesulfonyl azide 
• 84-65-1 9,10-phenanthrenequinone 
• 98-95-3 nitrobenzene 

Downstream Products

• 866998-65-4 N-(2-bromo-ethyl)-N-(9,10-dioxo-9,10-dihydro-[1]anthryl)-toluene-4-sulfonamide 
• 861608-05-1 1-(4-chloro-2-nitro-anilino)-anthraquinone 
• 2944-23-2 1-(4-nitro-anilino)-anthraquinone 
• 51970-60-6 1-(2-nitro-anilino)-anthraquinone 
• 2944-15-2 1-(4-amino-anilino)-anthraquinone 
• 51970-71-9 1-(2-amino-anilino)-anthraquinone 
• 82-45-1 1-amino-9,10-anthracenedione 

Relevant academic research and scientific papers

Ru(II)-catalyzed selective C-H amination of xanthones and chromones with sulfonyl azides: Synthesis and anticancer evaluation

A ketone-assisted ruthenium-catalyzed selective amination of xanthones and chromones C-H bonds with sulfonyl azides is described. The reactions proceed efficiently with a broad range of substrates with excellent functional group compatibility. This protoc

Synthesis and cytostatic activity of some sulfamido-anthraquinones

N-1- or 2-anthraquinonyl derivatives of p-methyl-, p-methoxy- and p- aminobenzenesulfonamides were synthesized and evaluated in vitro as antitumour agents. Only N-(1-anthraquinonyl)-p-methylbenzenesulfonamide (1) and -p- methoxy benzene sulfonamide deriva