1173913-69-3

Basic information

• Product Name: 2-methyl-3-((2-phenyl-1H-indol-3-yl)methyl)quinoline
• Synonyms: 2-methyl-3-((2-phenyl-1H-indol-3-yl)methyl)quinoline
• CAS NO: 1173913-69-3
• Molecular Weight: 348.447
• Mol File: 1173913-69-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-methyl-3-((2-phenyl-1H-indol-3-yl)methyl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-3-((2-phenyl-1H-indol-3-yl)methyl)quinoline(1173913-69-3)
• EPA Substance Registry System: 2-methyl-3-((2-phenyl-1H-indol-3-yl)methyl)quinoline(1173913-69-3)

Safety Data

• Hazardous Substances Data: 1173913-69-3(Hazardous Substances Data)

Upstream product

• 1173913-61-5 4-(2-nitrophenyl)-3-((2-phenyl-1H-indol-3-yl)methyl)but-3-en-2-one 
• 1401087-73-7 4-(2-nitrophenyl)-3-((2-phenyl-1H-indol-3-yl)methyl)-but-3-en-2-one 
• 948-65-2 2-phenyl-indole 
• 219982-00-0 3-[hydroxy-(2-nitrophenyl)methyl]but-3-en-2-one 

Relevant articles and documents

Synthesis of indolylquinolines, indolylacridines, and indolylcyclopenta[b] quinolines from the Baylis-Hillman adducts: An in situ [1,3]-sigmatropic rearrangement of an indole nucleus to access indolylacridines and indolylcyclopenta[b]quinolines

A simple and easy route to the synthesis of a variety of structurally diverse indolylquinolines, indolylacridines, and indolylcyclopenta[b]quinoline derivatives via the reductive cyclization of C-alkylated indole derivatives, derived from acyclic as well as cyclic Baylis-Hillman adducts with indoles, is described. An unusual in situ [1,3]-sigmatropic rearrangement of the indole nucleus was observed during the reductive cyclicization of α- regioselective B-H adducts containing indoles to produce indolylacridines and indolylcyclopenta[b]quinoline derivatives.