240417-42-9

Basic information

• Product Name: 1-(9-n-hexyl-9H-carbazol-3-yl)-2-phenylethane-1,2-dione
• Synonyms: 1-(9-n-hexyl-9H-carbazol-3-yl)-2-phenylethane-1,2-dione
• CAS NO: 240417-42-9
• Molecular Weight: 383.49
• Mol File: 240417-42-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(9-n-hexyl-9H-carbazol-3-yl)-2-phenylethane-1,2-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(9-n-hexyl-9H-carbazol-3-yl)-2-phenylethane-1,2-dione(240417-42-9)
• EPA Substance Registry System: 1-(9-n-hexyl-9H-carbazol-3-yl)-2-phenylethane-1,2-dione(240417-42-9)

Safety Data

• Hazardous Substances Data: 240417-42-9(Hazardous Substances Data)

Upstream product

• 240417-41-8 9-hexyl-3-(2-phenylethynyl)-9H-carbazole 
• 16807-13-9 3-iodocarbazole 
• 86-74-8 9H-carbazole 
• 156972-69-9 9-hexyl-3-iodo-9H-carbazole 

Downstream Products

• 240417-43-0 3-[3-(9-hexyl)carbazoyl]-2,4,5-triphenylcyclopenta-2,5-dien-1-one 

Relevant articles and documents

Ruthenium-catalyzed oxidation of alkynes to 1,2-diketones under room temperature and one-pot synthesis of quinoxalines

A ruthenium-catalyzed alkyne oxidation to 1,2-diketones using Oxone under room temperature is reported. Both substrate scope and mechanism were discussed. Notably, combination of the alkyne oxidation and condensation cyclization in one pot offers a very efficient and convenient entry into quinoxaline derivatives.

Improved Synthesis of Unsymmetrical, Heteroaromatic 1,2-Diketones and the Synthesis of Carbazole Ring Substituted Tetraaryl Cyclopentadieneones

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