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1-(4-imidazol-1-ylphenyl)imidazole is a chemical compound with the molecular formula C11H10N4. It is an imidazole derivative featuring a phenyl group and an imidazolyl group. 1-(4-imidazol-1-ylphenyl)imidazole is recognized for its potential therapeutic applications due to its ability to inhibit fungal growth and disrupt fungal cell membranes.

25372-07-0

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25372-07-0 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-imidazol-1-ylphenyl)imidazole is used as an antifungal agent for its effectiveness in treating various fungal infections such as athlete's foot and ringworm. It operates by inhibiting fungal growth and disrupting the integrity of fungal cell membranes, providing a therapeutic solution for these conditions.
Used in Research and Development:
1-(4-imidazol-1-ylphenyl)imidazole is utilized in scientific research for exploring its potential anti-inflammatory and anti-cancer properties. This makes it a versatile compound with a broad range of possible applications in the development of new treatments for inflammatory conditions and cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 25372-07-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 25372-07:
(7*2)+(6*5)+(5*3)+(4*7)+(3*2)+(2*0)+(1*7)=100
100 % 10 = 0
So 25372-07-0 is a valid CAS Registry Number.

25372-07-0SDS

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-(4-imidazol-1-ylphenyl)imidazole

1.2 Other means of identification

Product number -
Other names 1-[4-(1H-imidazol-1-yl)phenyl]-1H-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:25372-07-0 SDS

25372-07-0Relevant academic research and scientific papers

Polynuclear architectures with di- and tricarbene ligands

Rit, Arnab,Pape, Tania,Hahn, F. Ekkehardt

, p. 6393 - 6401 (2011)

The 1,3,5-triimidazolium-substituted benzene cation in H 3-1(PF6)3 reacts with Hg(OAc)2 to yield the cylinder-like trinuclear hexacarbene complex [Hg3(1) 2](PF6)6. Rea

Synthesis of binuclear palladium complexes with a rigid phenylene bridge linker

Wang, Guangying,Liu, Gang,Du, Yufeng,Li, Wenshu,Yin, Shuhui,Wang, Shuzhan,Shi, Yanhui,Cao, Changsheng

, p. 691 - 698 (2014)

The complexes [PdX2Py]2(di-NHC) (X = Br or Cl) in which di-NHC represents a di-N-heterocyclic carbene, featuring a rigid phenylene spacer between the carbene units, have been prepared from reactions of the corresponding diimidazolium

(CC*) Cyclometalated binuclear N-heterocyclic biscarbene platinum(ii) complexes-highly emissive phosphorescent emitters

Tronnier, Alexander,Strassner, Thomas

, p. 9847 - 9851 (2013)

A series of bimetallic N-heterocyclic carbene (NHC) platinum(ii) complexes with the general formula [Pt(NHC)(L)]2Ph were synthesized, which are composed of two [Pt(NHC)(L)] (L = acetylacetone, dipivaloylmethane or dimesitoylmethane; NHC = 3-met

Mesomorphic and ion conducting properties of dialkyl(1,4-phenylene) diimidazolium salts

Noujeim, Nadim,Samsam, Salim,Eberlin, Ludovic,Sanon, Samantha H.,Rochefort, Dominic,Schmitzer, Andreea R.

, p. 10914 - 10920,7 (2012)

A new family of dialkyl(1,4-phenylene)diimidazolium salts has been synthesized. Salts containing triflate and bis(trifluoromethanesulfonyl)imide anions and different alkyl chains have been prepared. The molecular structures of didodecyl(1,4-phenylene)diim

Tuning Gate-Opening of a Flexible Metal–Organic Framework for Ternary Gas Sieving Separation

Dong, Qiubing,Zhang, Xin,Liu, Shuang,Lin, Rui-Biao,Guo, Yanan,Ma, Yunsheng,Yonezu, Akira,Krishna, Rajamani,Liu, Gongpin,Duan, Jingui,Matsuda, Ryotaro,Jin, Wanqin,Chen, Banglin

, p. 22756 - 22762 (2020)

In comparison with the fast development of binary mixture separations, ternary mixture separations are significantly more difficult and have rarely been realized by a single material. Herein, a new strategy of tuning the gate-opening pressure of flexible

Covalent triazine frameworks for the selective sorption of palladium from highly acidic radioactive liquid wastes

Cai, Yimin,Feng, Wen,Liu, Hui,Qin, Song,Sun, Mengqi,Wu, Pengcheng,Ye, Jiawei,Yuan, Lihua,Zeng, Yaxin

supporting information, p. 27320 - 27331 (2021/12/24)

Efficient palladium recovery from high level liquid wastes (HLLW) is of increasing priority for sustainable development and addressing issues in radioactive waste treatment. However, searching for robust materials for palladium sorption, in the presence o

Nucleation of Tiny Silver Nanoparticles by Using a Tetrafacial Organic Molecular Barrel: Potential Use in Visible-Light-Triggered Photocatalysis

Mondal, Bijnaneswar,Bhandari, Pallab,Mukherjee, Partha Sarathi

supporting information, p. 15007 - 15015 (2020/10/19)

Coordination-driven self-assembly of discrete molecular architectures of diverse shapes and sizes has been well studied in the last three decades. Use of dynamic imine bonds for designing analogous metal-free architectures has become a growing challenge r

Ionic conductors containing phenyl/biphenyl and hydroxyalkyl as well as preparation method and application of ionic conductors

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Paragraph 0013, (2018/09/08)

The invention belongs to the technical field of organic photoelectric materials, particularly relates to functional ionic conductors as well as a preparation method and application thereof, and in particular relates to functionalized ionic conductors cont

Function-oriented ionic polymers having high-density active sites for sustainable carbon dioxide conversion

Chen, Yaju,Luo, Rongchang,Bao, Junhui,Xu, Qihang,Jiang, Jun,Zhou, Xiantai,Ji, Hongbing

, p. 9172 - 9182 (2018/05/28)

On the basis of the development of function-oriented synthesis (FOS), we presented for the first time an efficient and one-pot construction of functional ionic polymers (FIPs) through the phenol-formaldehyde condensation process (pre-synthetic approach); FIPs had high density of Br?nsted acidic and ionic sites. Considering the electrophilic-nucleophilic dual activation of phenolic hydroxyl groups and bromide anions, the imidazolium-based FIP-Im exhibited high activity for metal-, solvent- and additive-free synthesis of cyclic carbonates from CO2 and epoxides under mild conditions. Then, to obtain higher ionic density and a more flexible skeleton, FIP-Im@QA was also prepared by implanting quaternary ammonium (QA) in the framework of FIP-IMvia the Williamson ether synthesis (post-synthetic modification), which demonstrated high efficiency in the N-formylation reaction of multitudinous secondary amines with CO2 and PhSiH3 at ambient temperature. More interestingly, these function-oriented catalysts were compatible with the target transformation under low CO2 concentration (15% in 85% N2, v/v) and were also reused for more than six times without a significant loss of activity and selectivity. Therefore, this study could not only facilitate the design and construction of FIPs, but also provide sustainable protocols for efficient production of value-added chemicals from CO2 under mild conditions.

Metal complexes with di(N-heterocyclic carbene) ligands bearing a rigid: Ortho -, meta or para -phenylene bridge

Monticelli, Marco,Tubaro, Cristina,Baron, Marco,Basato, Marino,Sgarbossa, Paolo,Graiff, Claudia,Accorsi, Gianluca,Pell, Thomas P.,Wilson, David J. D.,Barnard, Peter J.

, p. 9540 - 9552 (2016/07/06)

Three novel dinuclear bis-dicarbene silver(i) complexes of general formula [Ag2(MeIm-phenylene-MeIm)2](PF6)2 (Im = imidazol-2-ylidene) were synthesized. The corresponding copper(i) and gold(i) complexes were obt

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