53676-68-9

Upstream product

• 1504-14-9 3,3-dimethylindolenine 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 53676-78-1 (2,3-dimethyl-1H-indol-1-yl)(4-nitrophenyl)methanone 
• 1174373-01-3 [3,3-dimethyl-2-(naphthalen-2-yloxy)indolin-1-yl](4-nitrophenyl)methanone 
• 1174372-95-2 [2-(4-methoxyphenoxy)-3,3-dimethylindolin-1-yl](4-nitrophenyl)methanone 
• 1174373-06-8 [2-(2-hydroxy-5-methoxyphenyl)-3,3-dimethylindolin-1-yl](4-nitrophenyl)methanone 
• 1174413-96-7 [2-(2-methoxynaphthalen-1-yl)-3,3-dimethylindolin-1-yl](4-nitrophenyl)methanone 
• 1174372-94-1 [3,3-dimethyl-2-(4-tolyloxy)indolin-1-yl](4-nitrophenyl)methanone 
• 1174372-98-5 [2-(2-hydroxy-5-methylphenyl)-3,3-dimethylindolin-1-yl](4-nitrophenyl)methanone 

Relevant academic research and scientific papers

Role of edge-to-face interaction between aromatic rings in clathrate formation of 1-benzoyl-2-hydroxyindoline derivatives with benzene. X-ray crystal and PM6 analyses of the interaction

(4-Nitrophenyl- and 4-chlorophenyl)(2-hydroxy-3,3-dimethylindolin-1-yl) methanone (4a,b) serve as clathrate hosts for benzene guests. X-ray crystal analyses of the inclusion compounds of 4a and 4b with benzene indicate that the 'edge-to-face interaction' plays an important role in the formation of the inclusion complexes with benzene as well as in the host-host interactions. PM6 molecular orbital calculations were found to reproduce the characteristic structural features of both intra- and intermolecular edge-to-face interactions.