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10040-96-7

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10040-96-7 Usage

General Description

1-(4-Bromophenyl)imidazole is a chemical compound that belongs to the class of organic compounds known as benzimidazoles. It is composed of a benzene ring fused with an imidazole ring, and has a bromine atom attached to the benzene ring. It has a molecular formula of C9H6BrN2 and generally exists as a white or off-white powder. Its melting point, boiling point, and specific gravity can vary depending upon purity and specific preparation methods. Being an imidazole derivative, it can be used in the synthesis of various pharmaceuticals and is also used in research as a building block for more complex chemical compounds. Its preparation involves specific organic reactions and strict handling, due to the involvement of bromine, which can be hazardous.

Check Digit Verification of cas no

The CAS Registry Mumber 10040-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,4 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10040-96:
(7*1)+(6*0)+(5*0)+(4*4)+(3*0)+(2*9)+(1*6)=47
47 % 10 = 7
So 10040-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrN2/c10-8-1-3-9(4-2-8)12-6-5-11-7-12/h1-7H

10040-96-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Bromophenyl)imidazole

1.2 Other means of identification

Product number -
Other names 1-(4-Bromophenyl)Imidazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10040-96-7 SDS

10040-96-7Relevant articles and documents

An efficient route to unsymmetrical bis(azolium) salts: CCC-NHC pincer ligand complex precursors

Box, Hannah K.,Howell, Tyler O.,Kennon, William E.,Burk, Griffin A.,Valle, Henry U.,Hollis, T. Keith

, p. 2191 - 2195 (2017)

The coupling of N-heterocyclic azoles (imidazoles, benzimidazoles, triazoles) to bromobenzenes (1,2-; 1,3-; or 1,4) in a step-wise, sequential manner was accomplished by manipulation of reaction time and stoichiometry, which provided straight-forward acce

Magnetic nano-Fe3O4 supported ionic liquids: A recoverable phase transfer catalyst for c-n cross coupling reaction

Tang, Lin,Sun, Yu,Zhou, Lingyun,Shao, Taili

, p. 6240 - 6242 (2013)

Magnetic nanoparticles-supported quaternary ammonium salts were prepared and evaluated as phase transfer catalysts. Some of them exhibited good activities in CuCl-catalyzed N-arylation of aryl amines and N-heterocycles with aryl iodides in aqueous solution without any ligands. They could be readily separated from reaction solution using an external magnet and reused three times with a little loss in activity.

3D printing of a heterogeneous copper-based catalyst

Tubío, Carmen R.,Azuaje, Jhonny,Escalante, Luz,Coelho, Alberto,Guitián, Francisco,Sotelo, Eddy,Gil, Alvaro

, p. 110 - 115 (2016)

One of the most important environmental challenges of modern society is to develop new catalysts that make possible chemical processes with reduced environmental impact. Catalyst immobilization is an appealing strategy that, in addition to facilitating catalyst recovery, has proved to give higher catalytic performance, since the solid support usually provides chemical, thermal, and mechanical stabilization to the catalytic species. In this work Cu/Al2O3 catalytic system with a woodpile porous structure is synthesized by 3D printing and then sintered at high temperature to generate a copper-supported rigid structure with high mechanical strength, a high surface-to-volume ratio, and controlled porosity. The catalytic species (Cu) are immobilized in the Al2O3 matrix to avoid the leaching of the metal into the reaction medium. Al2O3 was selected because it is a good material to obtain a structure with high mechanical stability after high-temperature treatment. The resulting device shows high catalytic efficacy and good recyclability and did not produce leaching of copper to the reaction medium in different Ullmann reactions. Ease of preparation, excellent reactivity, recyclability, and negligible metal contamination all make the 3D printing technique a good strategy for fabricating other types of metal/oxide heterogeneous catalytic systems.

The Catalytic Properties of a Copper-Based Nanoscale Coordination Polymer Fabricated by a Solvent-Etching Top-Down Route

Cao, Xiaowei,Fang, Zhenlan,Huang, Wei,Ju, Qiang

, p. 4803 - 4807 (2017)

Manipulating particle size is a powerful means of creating unprecedented applications in both inorganic and organic materials. Coordination polymers, which are emerging as a type of organic–inorganic hybrid materials, have attracted thriving interest in a variety of applications, but nanoscale coordination polymers have scarcely been touched. In this work, the pure-phase {Cu6[1,4-bis(imidazol-1-yl)butane]3I6}∞ coordination polymer with different sizes and morphologies was synthesized for the first time through a facile top-down route assisted by solvent etching. The size and morphology could be adjusted simply by varying the participating etching solvents. Our mechanistic investigations suggest that the bulk coordination polymer as a precursor in the etching solvents may experience a process of dispersion, dissolution, and recrystallization to generate the nanoscale counterpart. High catalytic activity of the nanoscale coordination polymer was observed in the N-arylation of imidazole aryl halides, and this was attributed to a high surface area and a low coordination number of unsaturated coordination sites. This simple and rapid preparation, requiring neither specialized equipment nor harsh conditions, suggests a wealth of potential for reducing the size of coordination polymers to comply with various practical applications.

Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles

Aghili, Nora,Hosseinzadeh, Rahman,Mavvaji, Mohammad

, (2022/01/03)

Functionalized nanocellulose was prepared and employed for immobilization of phenanthroline-copper(I) complex to afford cellulose nanofibril grafted heterogeneous copper catalyst [CNF-phen-Cu(I)]. This nanocatalyst was well characterized using FT-IR, NMR, XRD, CHNS, AAS, TGA, EDX and SEM. The activities of the synthesized catalyst were examined in the synthesis of diaryl ethers via C-O cross-coupling of phenols and aryl iodides, as well as, the preparation of N-aryl amides and N-aryl heterocycles through C-N cross-coupling of amides and N-H heterocycle compounds with aryl halides. In this trend, various substrates containing electron-donating and electron-withdrawing groups were exploited to evaluate the generality of this catalytic protocol. Accordingly, the catalyst demonstrated remarkable catalytic efficiency for both C-N and C-O cross-coupling reactions, thereby resulting in good to excellent yields of the desired products. Furthermore, the recoverability experiments of the catalyst showed that it can be readily retrieved by simple filtration and successfully reused several times with negligible loss of its catalytic activity.

Core-shell Cu2S:NiS2@C hybrid nanostructure derived from a metal-organic framework with graphene oxide for photocatalytic synthesis of N-substituted derivatives

Yusuf, Mohammad,Hira, Shamim Ahmed,Lim, Hyeonhan,Song, Sehwan,Park, Sungkyun,Park, Kang Hyun

, p. 9018 - 9027 (2021/04/16)

Recently, photocatalysis has attracted considerable interest, leading to opportunities for using renewable energy sources. A Cu:Ni metal-organic framework (MOF) modified with graphene oxide (GO) was fabricated by a facile and convenient process. Subsequen

Synthesis and Physical Properties of Tunable Aryl Alkyl Ionic Liquids (TAAILs)

Lerch, Swantje,Strassner, Thomas

supporting information, p. 15554 - 15557 (2021/10/06)

Tunable aryl alkyl ionic liquids (TAAILs) based on the imidazolium cation were first reported in 2009. Since then, a series of TAAILs with different properties due to the electron-donating or -withdrawing effect of the substituents at the aryl ring has be

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