72211-20-2

Upstream product

• 90534-62-6 2-(2-oxopropyl)cyclohexane-1,3-dione 
• 62-53-3 aniline 
• 16868-65-8 2-(prop-2-yn-1-yl)cyclohexane-1,3-dione 
• 504-02-9 1,3-cylohexanedione 
• 1265166-83-3 3-(phenylamino)-2-(prop-2-ynyl)cyclohex-2-enone 
• 73336-28-4 2-(2-bromoprop-2-en-1-yl)cyclohexane-1,3-dione 

Downstream Products

• 1026723-62-5 5-allyl-2-methyl-1-phenyl-4,5,6,7-tetrahydro-1H-4-indolone 
• 72211-21-3 1,5,6,7-Tetrahydro-5-hydroxymethylen-2-methyl-1-phenylindol-4-on 
• 853730-77-5 4-chloro-2-methyl-1-phenyl-6,7-dihydro-1H-indole-5-carbaldehyde 
• 916609-72-8 5-carbaldehyde-4-hydroxy-2-methyl-1-phenyl-6,7-dihydro-1H-indole 
• 1354789-58-4 C₄₈H₃₈N₄ 
• 1026307-41-4 2-methyl-1-phenyl-5-(2-oxopropyl)-4,5,6,7-tetrahydro-1H-4-indolone 
• 853730-80-0 4-(ethylsulfanyl)-2-methyl-1-phenyl-6,7-dihydro-1H-indole-5-carbaldehyde 
• 853730-83-3 4-(ethylsulfanyl)-2-methyl-1-phenyl-1H-indole-5-carbaldehyde 
• 606932-55-2 3-benzoyl-8-methyl-7-phenyl-5,7-dihydro-1H,6H-pyrrolo[2,3-h]quinolin-2-one 
• 606932-54-1 3-benzenesulfonyl-8-methyl-7-phenyl-5,7-dihydro-1H,6H-pyrrolo[2,3-h]quinolin-2-one 
• 606932-56-3 8-methyl-2-oxo-7-phenyl-2,5,6,7-tetrahydro-1H-pyrrolo[2,3-h]quinoline-3-carbonitrile 
• 606932-63-2 5-[(diethylamino)methylidene]-2-methyl-1-phenyl-1,5,6,7-tetrahydro-4H-indol-4-one 

Relevant academic research and scientific papers

NOVEL ORGANIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

The present invention provides a blue or green phosphorescent organic electroluminescent device which has high luminous efficiency. An organic electroluminescent device includes a light-emitting layer containing a pyrroloindole compound represented by gen

Iron-catalyzed synthesis of polysubstituted pyrroles via [4C+1N] cyclization of 4-acetylenic ketones with primary amines

A highly efficient iron-catalyzed approach to polysubstituted pyrroles has been developed through the [4C+1N] cyclization of 4-acetylenic ketones with primary amines, leading to the synthesis of a variety of tetra- and fully-substituted pyrroles as well a

Pyrrolo[2,3-h]quinolinones: Synthesis and photochemotherapic activity

A series of derivatives of the new ring system pyrrolo[2,3-h]quinoline-2-one was synthesized and evaluated as photoreagents toward cultured human tumor cells. Remarkable phototoxycity resulted for some derivatives, especially those bearing the phenyl grou

Synthesis of 1,2,3,5-tetrasubstituted pyrrole derivatives from 2-(2-bromoallyl)-1,3-dicarbonyl compounds

2-(2-Bromoallyl)-1,3-dicarbonyl compounds are converted into β-enamino, β-hydrazino esters and ketones, followed by base-promoted cyclization, leading to the formation of the corresponding 1,2,3,5-tetrasubstituted pyrroles. 1,2,4- and 1,2,3,4-Substituted pyrroles are also isolated as minor products. Starting from the 2-(2-bromoallyl)-cyclohexane-1,3-dione the corresponding tetrahydro indolone is prepared in good yield.

1,3-Cyclohexanedione as the precursor of C4X-C6-C4Y systems. Synthesis of pyrrolo[2,3-e]indoles and thieno[2,3-e]indoles

A novel synthesis of substituted pyrrolo[2,3-e]indoles and thieno[2,3- e]indoles is described. This new approach uses 1,3-cyclohexanedione as the starting material. Diketone intermediates are obtained in four steps from the aforementioned ketone. Using these intermediates, the title compounds are synthesized efficiently.