10041-03-9

Basic information

• Product Name: Phenol, 3-(1H-imidazol-1-yl)-
• CAS NO: 10041-03-9
• Molecular Formula: C9H8N2O
• Molecular Weight: 160.175
• Mol File: 10041-03-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Phenol, 3-(1H-imidazol-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-(1H-imidazol-1-yl)-(10041-03-9)
• EPA Substance Registry System: Phenol, 3-(1H-imidazol-1-yl)-(10041-03-9)

Safety Data

• Hazardous Substances Data: 10041-03-9(Hazardous Substances Data)

Upstream product

• 10040-94-5 1-(3-methoxyphenyl)-1H-imidazole 
• 288-32-4 1H-imidazole 
• 2398-37-0 3-methoxyphenyl bromide 
• 87199-18-6 3-hydroxyphenylboronic acid 
• 591-20-8 3-Bromophenol 
• 822-36-6 4-methyl-1H-imidazole 
• 536-90-3 m-Anisidine 

Downstream Products

• 1192322-86-3 C₁₃H₁₇N₂O⁽¹⁺⁾*I^(1-) 
• 1442663-44-6 1-methyl-3-(3-hydroxyphenyl)imidazolium iodide 
• 1192322-87-4 1-butyl-3-(3-(di-tert-butylphosphinooxy)phenyl)imidazolium iodide 
• 1442663-39-9 1-methyl-3-(3-(di-tert-butylphosphinooxy)-phenyl)imidazolium iodide 
• 1448175-15-2 2-(3-(3-(1H-imidazol-1-yl)phenoxy)phenoxy)pyridine 

Relevant articles and documents

Nano copper(i) oxide/zinc oxide catalyzed N-arylation of nitrogen-containing heterocycles with aryl halides and arylboronic acids in air

The synergistic effect of zinc and copper in Cu2O/ZnO nanoflake as a heterogeneous catalyst for the N-arylation of heterocycles with aryl halides and arylboronic acids in the absence of additional ligand in air were demonstrated. The catalyst was characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), BET surface area measurement, and FT-IR spectroscopy. The Royal Society of Chemistry 2014.

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

An organic light-emitting device is provided to include: a first electrode; a second electrode facing the first electrode; an organic layer between the first electrode and the second electrode, the organic layer including an emission layer; and at least o

N-(1-Oxy-2-picolyl)oxalamic acids as a new type of O,O-ligands for the Cu-catalyzed N-arylation of azoles with aryl halides in water or organic solvent

N-(1-Oxy-pyridin-2-ylmethyl)oxalamic acids (L3-L5) were identified as novel efficient ligands for copper-catalyzed C-N cross-coupling of azoles and aryl halides in water. The N-arylation of imidazoles, indoles and pyrazoles proceeded with moderate to excellent yields and complete selectivity over aromatic amines and phenols. Moreover, L5, which is also efficient in organic solvent with low catalyst loading, can be used to promote the N-arylation reactions with water-sensitive materials. The catalytic mechanism was proposed based on the results of several verification experiments which indicated that the ligands as new-type chelators may coordinate to Cu(i) with two oxygen atoms of N-oxide and amide in the coupling process. This journal is