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25372-02-5

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25372-02-5 Usage

General Description

1-(3-bromophenyl)-1H-imidazole is a chemical compound with the formula C9H7BrN2. It is a white to off-white crystalline powder that is sparingly soluble in water. 1-(3-bromophenyl)-1H-imidazole is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in research and development of new medications. It is also utilized as an intermediate in the production of various organic compounds. 1-(3-bromophenyl)-1H-imidazole is known to have antimicrobial and antifungal properties, making it useful in the development of antimicrobial agents. Additionally, it has been investigated for its potential use in various medical applications, such as treating fungal infections and as an antifungal coating for medical devices.

Check Digit Verification of cas no

The CAS Registry Mumber 25372-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25372-02:
(7*2)+(6*5)+(5*3)+(4*7)+(3*2)+(2*0)+(1*2)=95
95 % 10 = 5
So 25372-02-5 is a valid CAS Registry Number.

25372-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)imidazole

1.2 Other means of identification

Product number -
Other names -

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:25372-02-5 SDS

25372-02-5Downstream Products

25372-02-5Relevant articles and documents

Advantages of organic halogen bonding for halide recognition

Wageling, Nicholas B.,Neuhaus, George F.,Rose, Ariana M.,Decato, Daniel A.,Berryman, Orion B.

, p. 665 - 672 (2016)

The synthesis of a bidentate halogen bonding receptor and a nearly isostructural hydrogen bonding analogue is described. Crystal structures reveal the interactions of each receptor with anions in the solid state, while NMR titrations elucidate bidentate binding and association constants in solution. Of the two, the halogen bonding receptor demonstrates stronger, water resistant halide binding in competitive solvents.

Immobilization of copper(II) into polyacrylonitrile fiber toward efficient and recyclable catalyst in Chan-Lam coupling reactions

Zhang, Chenlu,Zhu, Hai,Gang, Kaiyue,Tao, Minli,Ma, Ning,Zhang, Wenqin

, (2021/02/09)

A series of polyacrylonitrile fiber (PANF)-supported copper(II) catalysts were prepared through the immobilization of Cu(II) into prolinamide-modified PANF (PANPA-2F) and subsequently used for the synthesis of diverse N-arylimidazoles from arylboronic acids and imidazole. The prepared Cu(II)@PANPA-2Fs were well characterized by mechanical strength, FT-IR, XRD, XPS and SEM. Among them, CuCl2@PANPA-2F exhibited excellent catalytic performance, and its activity was significantly affected by the Cu loading. This catalytic system also displayed good activity in the synthesis of N-arylsulfonamides from arylboronic acids and tosyl azide. It was highly efficient in gram-scale reactions and could be reused five times. The advantages of low cost, easy preparation, good durability and facile recovery make the fiber catalyst attractive.

Organometallic compound, organic light-emitting device including the same and apparatus including the same

-

Paragraph 0644-0647, (2021/01/01)

Provided are an organometallic compound, an organic light-emitting device including the organometallic compound, and an apparatus including the organometallic compound. The organic light-emitting device includes a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode and including an emission layer, wherein the organic layer includes the organometallic compound.

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