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66631-29-6

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66631-29-6 Usage

General Description

4-(1H-Benzoimidazol-2-yl)-benzoic acid is a compound with the molecular formula C15H11N3O2. It is a derivative of benzoic acid and contains a benzimidazole ring. 4-(1H-Benzoimidazol-2-yl)-benzoic acid has been studied for its potential pharmacological properties, including its ability to bind to certain receptors and enzymes in the body. It has also been investigated for its potential use in the development of new drugs for various medical conditions. The chemical structure and properties of 4-(1H-Benzoimidazol-2-yl)-benzoic acid make it a subject of interest for researchers in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 66631-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66631-29:
(7*6)+(6*6)+(5*6)+(4*3)+(3*1)+(2*2)+(1*9)=136
136 % 10 = 6
So 66631-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O2/c17-14(18)10-7-5-9(6-8-10)13-15-11-3-1-2-4-12(11)16-13/h1-8H,(H,15,16)(H,17,18)

66631-29-6Downstream Products

66631-29-6Relevant articles and documents

4-(1H-benzimidazol-3-ium-2-yl)-benzoate dihydrate

Jian, Fangfang,Bei, Fengli,Yang, Xujie,Lu, Lude,Wang, Xin,Razak, Ibrahim Abdul,Sundara Raj, S. Shanmuga,Fun, Hoong-Kun

, p. 176 - 177 (2001)

In the title compound, C14H10N2O2·2H2O, the water molecules are involved in hydrogen bonds and interactions. Intermolecular and intramolecular O-H...O hydrogen bonds connect the complex into chains along the a axis, whereas N-H...O intermolecular hydrogen bonds and C-H...O interactions interconnect these layers forming a three-dimensional network.

UV-visible light-induced photochemical synthesis of benzimidazoles by coomassie brilliant blue coated on W-ZnO@NH2nanoparticles

Chen, Ruijuan,Jalili, Zahra,Tayebee, Reza

, p. 16359 - 16375 (2021/05/19)

Heterogeneous photocatalysts proffer a promising method to actualize eco-friendly and green organic transformations. Herein, a new photochemical-based methodology is disclosed in the preparation of a wide range of benzimidazoles through condensation of o-phenylenediamine with benzyl alcohols in the air under the illumination of an HP mercury lamp in the absence of any oxidizing species catalyzed by a new photocatalyst W-ZnO@NH2-CBB. In this photocatalyst, coomassie brilliant blue (CBB) is heterogenized onto W-ZnO@NH2 to improve the surface characteristics at the molecular level and enhance the photocatalytic activity of both W-ZnO@NH2 and CBB fragments. This unprecedented heterogeneous nanocatalyst is also identified by means of XRD, FT-IR, EDS, TGA-DTG, and SEM. The impact of some influencing parameters on the synthesis route and effects on the catalytic efficacy of W-ZnO@NH2-CBB are also assessed. The appropriate products are attained for both the electron-withdrawing and electron-donating substituents in the utilized aromatic alcohols. Furthermore, preparation of benzimidazoles is demonstrated to occur mainly via a radical mechanism, which shows that reactive species such as ·O2-, OH and h+ would be involved in the photocatalytic process. Stability and reusability studies also warrant good reproducibility of the nanophotocatalyst for at least five runs. Eventually, a hot filtration test proved that the nanohybrid photocatalyst is stable in the reaction medium. Using an inexpensive catalyst, UV-vis light energy and air, as a low cost and plentiful oxidant, puts this methodology in the green chemistry domain and energy-saving organic synthesis strategies. Finally, the anticancer activity of W-ZnO nanoparticles is investigated on MCF7 breast cancer cells by MTT assay. This experiment reveals that the mentioned nanoparticles have significant cytotoxicity towards the selected cell line.

Selective photocatalytic oxidation of aromatic alcohols to aldehydes with air by magnetic WO3ZnO/Fe3O4.: In situ photochemical synthesis of 2-substituted benzimidazoles

Esmaeili, Effat,Li, Bozhi,Maleki, Behrooz,Namaghi, Mina S.,Tayebee, Reza

, p. 40725 - 40738 (2020/11/23)

Recently, visible light-driven organic photochemical synthesis has been a pioneering field of interest from academic and industrial associations due to its unique features of green and sustainable chemistry. Herein, WO3ZnO/Fe3O4 was synthesized, characterized, and used as an efficient magnetic photocatalyst in the preparation of a range of 2-substituted benzimidazoles via the condensation of benzyl alcohol and o-phenylenediamine in ethanol at room temperature for the first time. The key feature of this work is focused on the in situ photocatalytic oxidation of benzyl alcohols to benzaldehydes under atmospheric air and in the absence of any further oxidant. This new heterogeneous nanophotocatalyst was characterized via XRD, FT-IR, VSM and SEM. Short reaction time, cost-effectiveness, broad substrate scope, easy work-up by an external magnet, and excellent product yield are the major advantages of the present methodology. A number of effective experimental parameters were also fully investigated to clear broadness and generality of the protocol. This journal is

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