500992-15-4

Upstream product

• 64890-06-8 7-nitro-2-phenylindole 
• 536-74-3 phenylacetylene 
• 500992-09-6 N-[(6'-nitro-2'-phenylethynyl)phenyl]butyramide 

Downstream Products

• 870820-07-8 N-(2-phenylindol-7-yl)-4-toluenesulfonamide 
• 870820-08-9 N-(2-phenylindol-7-yl)-4-methoxybenzenesulfonamide 
• 1253395-99-1 N-(3-formyl-2-phenylindol-7-yl)-4-methoxybenzenesulfonamide 
• 1253396-00-7 N-(3-hydroxymethyl-2-phenylindol-7-yl)-4-methoxybenzenesulfonamide 
• 1253395-96-8 N-(3-piperidinomethyl-2-phenylindol-7-yl)-4-methoxybenzenesulfonamide 
• 1253395-98-0 N-[3-(4-morpholino)methyl-2-phenylindol-7-yl]-4-methoxybenzenesulfonamide 

Relevant academic research and scientific papers

Synthesis of anti-microtubule N-(2-arylindol-7-yl)-benzenesulfonamide derivatives and their antitumor mechanisms

Breaking the cycle: A series of N-(2-arylindol-7-yl)benzenesulfonamide derivatives were prepared. Among them, compound 2 showed promising antiproliferative activity against hormone-resistant prostate cancer PC-3 cells, induced G2/M-phase arrest

Chemistry of aminophenols. Part 2: A general and efficient synthesis of indoles possessing a nitrogen substituent at the C4, C5, C6, and C7 positions

A general and efficient synthesis of indoles possessing a nitrogen substituent at the C4, C5, C6, and C7 positions has been developed. Starting from commercially available nitro 2-aminophenols, 5-, 6-, and 7-arenesulfamoylindoles were synthesized via a ba