1242139-62-3

Basic information

• Product Name: 1-(benzyloxy)-6-methylnaphtho[2,3-a]carbazole-5,13-dione
• Synonyms: 1-(benzyloxy)-6-methylnaphtho[2,3-a]carbazole-5,13-dione
• CAS NO: 1242139-62-3
• Molecular Weight: 417.464
• Mol File: 1242139-62-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(benzyloxy)-6-methylnaphtho[2,3-a]carbazole-5,13-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxy)-6-methylnaphtho[2,3-a]carbazole-5,13-dione(1242139-62-3)
• EPA Substance Registry System: 1-(benzyloxy)-6-methylnaphtho[2,3-a]carbazole-5,13-dione(1242139-62-3)

Safety Data

• Hazardous Substances Data: 1242139-62-3(Hazardous Substances Data)

Upstream product

• 7479-20-1 N-methyl-3-(indol-3-yl)propionic acid 
• 119650-41-8 5-(benzyloxy)-2-bromonaphthalene-1,4-dione 

Relevant articles and documents

One-pot three-step synthesis of naphtho[2,3-α]carbazole5,13-diones using a tandem radical alkylation-cyclization-aromatization reaction sequence

A three-step, one-pot tandem reaction including radical nucleophilic alkylation/cyclization/ aromatization was developed using 0.3 equivalents of silver(I) acetate (AgOAc) as the catalyst and 2 equivalents of ammonium persulfate [(NH4)2S2O8] as the oxidant. This strategy is highly efficient for the assembly of pentacyclic complex carbazoles from aryl-fused bromobenzoquinones and indol-3ylpropanoic acid acids in 52-72% overall yields (three steps). This new approach provides a significant improvement over the previously reported methods and would greatly facilitate analog library construction of pentacyclic complex carbazoles and benefit further biological evaluation of these compounds.