132554-37-1

Basic information

• Product Name: 1,7-dimethyl-2-phenyl-1H-indole
• Synonyms: 1,7-dimethyl-2-phenyl-1H-indole
• CAS NO: 132554-37-1
• Molecular Weight: 221.302
• Mol File: 132554-37-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,7-dimethyl-2-phenyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 1,7-dimethyl-2-phenyl-1H-indole(132554-37-1)
• EPA Substance Registry System: 1,7-dimethyl-2-phenyl-1H-indole(132554-37-1)

Safety Data

• Hazardous Substances Data: 132554-37-1(Hazardous Substances Data)

Upstream product

• 5621-16-9 1,7-dimethyl-1H-indole 
• 98-80-6 phenylboronic acid 
• 98-86-2 acetophenone 
• 529-27-1 2-methylphenylhydrazine 
• 59541-82-1 7-methyl-2-phenyl-1H-indole 
• 74-88-4 methyl iodide 
• 933-67-5 7-methyl-1H-indole 
• 591-50-4 iodobenzene 
• 2996-92-1 phenyl trimethylsiloxane 
• 132554-26-8 3-(3-Methyl-pyridin-2-yl)-1-phenyl-propan-1-one 
• 108-86-1 bromobenzene 
• 132554-30-4 1,3-Dimethyl-2-(2-benzoylethyl)pyridinium iodide 
• 74-89-5 methylamine 

Relevant articles and documents

In Situ Preparation of Palladium Nanoparticles for C-2 Selective Arylation of Indoles in Agro-Waste Extract Based Mixed Solvents

An efficient and practical method for the in situ generation of palladium nanoparticles was successfully established in a water extract of pomelo peel ash. The produced palladium nanoparticles were characterized by energy-dispersive X-ray spectroscopy elemental mapping, field emission scanning electron microscopy, high-resolution transmission electron microscope, X-ray powder diffraction, and showed high catalytic activity for selective C-2 arylation of indoles. A series of 2-arylindoles were smoothly installed in moderate to good yields through the direct palladium-catalyzed cross-coupling reactions of indoles and iodoarenes without external ligand, base, oxidant, and preinstallation directing group.

A Three-Component Strategy for Benzoselenophene Synthesis under Metal-Free Conditions Using Selenium Powder

An efficient three-component benzoselenophenes formation has been developed from substituted indoles, acetophenones, and selenium powder under metal-free conditions. 2-Aryl indoles played an important role to promote benzoselenophene formation from acetophenone derivatives and selenium powder. One C-C and two C-Se bonds were selectively formed to provide 40 new benzoselenophenes in good yields.

Pd(OAc)2-catalyzed regioselective arylation of indoles with arylsiloxane in acidic medium

(Figure Presented) Mild conditions have been developed to achieve a Pd(OAc)2-catalyzed cross-coupling between indoles and arylsiloxanes in the presence of TBAF and Ag2O in acidic medium. Electron-deficient arylsiloxanes presented high efficiency in this system to give the arylated indoles in excellent yields.