1401087-68-0

Basic information

• Product Name: 3-((1H-indol-3-yl)methyl)-4-(2-nitrophenyl)but-3-en-2-one
• Synonyms: 3-((1H-indol-3-yl)methyl)-4-(2-nitrophenyl)but-3-en-2-one
• CAS NO: 1401087-68-0
• Molecular Weight: 320.348
• Mol File: 1401087-68-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-((1H-indol-3-yl)methyl)-4-(2-nitrophenyl)but-3-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((1H-indol-3-yl)methyl)-4-(2-nitrophenyl)but-3-en-2-one(1401087-68-0)
• EPA Substance Registry System: 3-((1H-indol-3-yl)methyl)-4-(2-nitrophenyl)but-3-en-2-one(1401087-68-0)

Safety Data

• Hazardous Substances Data: 1401087-68-0(Hazardous Substances Data)

Upstream product

• 120-72-9 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.