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100726-39-4

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100726-39-4 Usage

General Description

(2-PYRIDIN-2-YL-BENZOIMIDAZOL-1-YL)-ACETIC ACID is a chemical compound with the molecular formula C14H11N3O2. It is a derivative of benzoimidazole and pyridine, containing an acetic acid functional group. (2-PYRIDIN-2-YL-BENZOIMIDAZOL-1-YL)-ACETIC ACID is used in various pharmaceutical and medicinal applications, including as an inhibitor of certain enzymes and as a potential therapeutic agent for the treatment of various diseases. Its specific properties and potential uses in the field of medicine make it an important compound for research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 100726-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100726-39:
(8*1)+(7*0)+(6*0)+(5*7)+(4*2)+(3*6)+(2*3)+(1*9)=84
84 % 10 = 4
So 100726-39-4 is a valid CAS Registry Number.

100726-39-4Downstream Products

100726-39-4Relevant articles and documents

Ruthenium complexes of 2-(2′-pyridyl)benzimidazole as photosensitizers for dye-sensitized solar cells

Yi, Hunan,Crayston, Joe A.,Irvine, John T.S.

, p. 685 - 691 (2003)

N-Alkylated carboxylic acid derivatives of 2-(2′-pyridyl)benzimidazole (pbimH) with different chain-lengths (pbim(CH)nCO2H where n = 1-3) and their ruthenium complexes [Ru(bpy)2(pbim)](PF6)2 have been synthesized and characterized. 2D COSY and NOESY NMR spectroscopy were used to aid the assignment of the pbim NMR spectrum. The effect of chain-length on the cyclic voltammetry (CV) was studied and the voltammetry of the parent pbimH complex was re-investigated. The ability of the carboxylic acid groups to bind to TiO2 coated electrodes was confirmed by the observation of a symmetrical, surface-confined RuIII/II wave, while the specular reflectance IR revealed a band at 1620 cm-1 due to the bound carboxylate (COO ... Ti) group. The efficiencies of solar cells using these sensitizers were rather low, due to the distance between the sensitizer and the surface and the inefficient coupling of the charge-separated excited state to the surface. A fall in the cell open-circuit voltage with chain length reflected this distance effect. Time-resolved luminescence spectroscopy indicated that rapid electron injection into the TiO2 conduction band was occurring (30 ns), but this is not fast enough to compete effectively with alternative excited state processes.

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