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1-(2-(1H-imidazol-1-yl)phenyl)-1H-imidazole is a heterocyclic organic compound characterized by its molecular formula C13H11N3. It features two imidazole rings and a phenyl group, which contribute to its diverse range of biological activities and potential applications in various fields.

137494-64-5

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137494-64-5 Usage

Uses

Used in Medicinal Chemistry and Pharmaceuticals:
1-(2-(1H-imidazol-1-yl)phenyl)-1H-imidazole is utilized as a drug candidate in the medicinal chemistry and pharmaceutical industries due to its antiviral, antibacterial, and antifungal properties. It is being studied for its potential in treating a variety of diseases, making it a promising compound for drug discovery and development.
Used in Research Laboratories:
In addition to its pharmaceutical applications, 1-(2-(1H-imidazol-1-yl)phenyl)-1H-imidazole is also employed as a reagent in organic synthesis within research laboratories. Its unique structure allows it to serve as a building block for the preparation of various functionalized compounds, further expanding its utility in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 137494-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,9 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137494-64:
(8*1)+(7*3)+(6*7)+(5*4)+(4*9)+(3*4)+(2*6)+(1*4)=155
155 % 10 = 5
So 137494-64-5 is a valid CAS Registry Number.

137494-64-5Relevant academic research and scientific papers

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)

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

Bimetallic N-Heterocyclic Carbene Rh(I) Complexes: Probing the Cooperative Effect for the Catalyzed Hydroelementation of Alkynes

Diachenko, Vera,Page, Michael J.,Gatus, Mark R. D.,Bhadbhade, Mohan,Messerle, Barbara A.

, p. 4543 - 4552 (2015)

A series of bimetallic N-heterocyclic carbene Rh(I) complexes (13, 14, 16, 18, 19, and 21) were prepared, in which two metal fragments are linked to a central organic scaffold. These complexes were investigated as catalysts for the hydroelementation of al

Copper(I)-catalyzed cycloaddition of 4-bromosydnones and alkynes for the regioselective synthesis of 1,4,5-trisubstituted pyrazoles

Decuypere, Elodie,Specklin, Simon,Gabillet, Sandra,Audisio, Davide,Liu, Hui,Plougastel, Lucie,Kolodych, Sergii,Taran, Frédéric

supporting information, p. 362 - 365 (2015/01/30)

Copper-catalyzed cycloaddition of alkynes with 4-bromosydnones provides a convenient, mild, and regioselective method for the synthesis of a wide range of bromopyrazoles. The broad functional group tolerance of the cycloaddition reaction and further palla

Novel formation of diimidazo[1,2-a:2′,1′-c]quinoxaline derivatives and their optical properties

Matsumoto, Shoji,Batmunkh, Erdenebolor,Akazome, Motohiro,Takata, Yoshiyuki,Tamano, Michiko

supporting information; experimental part, p. 5941 - 5944 (2011/10/10)

Reaction of 1,2-di(imidazolyl)benzene treated with n-BuLi proceeded to give diimidazo[1,2-a:2′,1′-c]quinoxaline in the presence of iodine or Pd(PPh3)4. Blue fluorescence was observed from 3,10-diarylated diimidazoquinoxalines with hi

Helical nonracemic tubular coordination polymer gelators from simple achiral molecules

Zhang, Shiyong,Yang, Shengyong,Lan, Jingbo,Yang, Shuaijun,You, Jingsong

supporting information; experimental part, p. 6170 - 6172 (2009/05/06)

A novel class of helical nonracemic tubular coordination polymers, which can immobilize a wide range of solvents at very low concentrations, have been synthesized for the first time in the absence of chiral influences and appended groups. The Royal Societ

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