238398-37-3

Upstream product

• 1407182-07-3 C₁₆H₁₀ClF₃N₂O 
• 412947-46-7 4-chloro-2-ethynylaniline 
• 143321-89-5 2,2,2-trifluoro-N-(2-iodophenyl)acetamide 
• 551-93-9 2-aminoacetophenone 

Downstream Products

• 238398-44-2 N-[2-(5-chloro-1H-indol-2-yl)phenyl]acetamide 
• 238398-56-6 2-(2-aminophenyl)-5-chloro-3-nitrosoindole 
• 238398-50-0 2-(2-acetylaminophenyl)-5-chloro-3-nitrosoindole 
• 1449134-93-3 1-((2'R,3'S)-3',5'-dichloro-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indolin]-1'-yl)ethanone 
• 1449135-05-0 N-(2-(1-acetyl-5-chloro-1H-indol-2-yl)phenyl)benzamide 

Relevant academic research and scientific papers

Selective C?H or N?H Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds

2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic C?H and indolo N?H functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl

Palladium(II)-catalyzed cycloamidination via C(sp2)-H activation and isocyanide insertion

An efficient method for the synthesis of nitrogen heterocycles containing a cyclic amidine moiety has been developed. The process involves palladium-catalyzed C(sp2)-H activation and isocyanide insertion starting with readily accessible ortho-heteroarene-substituted aniline derivatives under mild conditions. Copyright

Derivatives of the new ring system indolo[1,2-c]benzo[1,2,3]triazine with potent antitumor and antimicrobial activity

Derivatives of the new ring system indolo[1,2-c]benzo[1,2,3]triazine 5 were synthesized by diazotization of substituted 2-(2-aminophenyl)indoles followed by an intramolecular coupling reaction of the diazonium group with the indole nitrogen. To obtain the