210162-61-1

Basic information

• Product Name: 1H-Indole, 1-(2-Methylphenyl)-
• Synonyms: 1H-Indole, 1-(2-Methylphenyl)-;1-o-Tolyl-1H-indole
• CAS NO: 210162-61-1
• Molecular Formula: C₁₅H₁₃N
• Molecular Weight: 207.27042
• Mol File: 210162-61-1.mol
• Article Data: 24

Chemical Properties

• Melting Point: 201-203 °C
• Boiling Point: 347.0±25.0 °C(Predicted)
• Appearance: /
• Density: 1.04±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1H-Indole, 1-(2-Methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 1-(2-Methylphenyl)-(210162-61-1)
• EPA Substance Registry System: 1H-Indole, 1-(2-Methylphenyl)-(210162-61-1)

Safety Data

• Hazardous Substances Data: 210162-61-1(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 615-37-2 ortho-methylphenyl iodide 
• 16419-60-6 2-Methylphenylboronic acid 
• 1477-50-5 Indole-2-carboxylic acid 
• 95-46-5 2-methylphenyl bromide 
• 625-95-6 3-Iodotoluene 
• 95-53-4 o-toluidine 

Downstream Products

• 1238393-16-2 (+/-)-N-(2'-methylphenyl)-2-diphenylphosphinoindole 

Relevant articles and documents

Exploration of Catalytic Activity of Quercetin Mediated Hydrothermally Synthesized NiO Nanoparticles Towards C–N Coupling of Nitrogen Heterocycles

Abstract: A new approach towards the preparation of phase pure NiO nanoparticles via quercetin mediated hydrothermal method is proposed in this work. The performance of quercetin as capping agent is found to be good. The XRD and SEM results confirm that the NiO nanoparticles prepared with quercetin are smaller in size and have refined morphology than that prepared without quercetin. Thermal stability, elemental composition and particle size of prepared nanoparticles have been revealed by TG-DSC, EDAX and HR-TEM analysis respectively. N2 adsorption–desorption isotherm (BET) analysis was done to reveal specific surface area. The prepared NiO nanoparticles act as cost effective, environmental friendly and efficient catalyst for the C–N cross coupling of indole and electron deficient pyrrole, under very mild reaction conditions. The catalytic system is able to tolerate many functional groups with different electronic and structural properties. Hence the present catalytic system may be possibly applied in large scale synthesis. Graphic Abstract: [Figure not available: see fulltext.].

Iron oxide encapsulated by copper-Apatite: An efficient magnetic nanocatalyst for: N-Arylation of imidazole with boronic acid

N-Arylation of imidazole was carried out with various arylboronic acids on iron oxide encapsulated by copper-Apatite (Fe3O4?Cu-Apatite), producing excellent yields. Firstly, the iron nanoparticles were prepared using a solvothermal m

Copper(I) Oxide/N,N′-Bis[(2-furyl)methyl]oxalamide-Catalyzed Coupling of (Hetero)aryl Halides and Nitrogen Heterocycles at Low Catalytic Loading

An easily prepared oxalic diamide is a powerful ligand for the copper-catalyzed coupling of aryl halides with nitrogen heterocycles. Only 1–2 mol% each of copper(I) oxide and N,N′-bis[(2-furyl)methyl]oxalamide (BFMO) are needed to form N-arylation products under mild conditions. More than 10 different types of nitrogen heterocycles are compatible with these conditions, thereby giving the corresponding N-arylation products. (Figure presented.).