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[Fe(η(5)-C5H5)(η(5)-C5H4C6H4N=CHC5H4N)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159541-67-0

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159541-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159541-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159541-67:
(8*1)+(7*5)+(6*9)+(5*5)+(4*4)+(3*1)+(2*6)+(1*7)=160
160 % 10 = 0
So 159541-67-0 is a valid CAS Registry Number.

159541-67-0Relevant academic research and scientific papers

Synthesis, physical and antimicrobial studies of ferrocenyl-N-(pyridinylmethylene)anilines and ferrocenyl-N-(pyridinylmethyl)anilines

Njogu, Eric M.,Omondi, Bernard,Nyamori, Vincent O.

, p. 51 - 66 (2016/11/11)

Ferrocenyl-N-(pyridinylmethylene)anilines Schiff bases were synthesized by reaction of 3- or 4-ferrocenylaniline with either 2-, 3-, or 4-pyridinecarboxaldehyde under solvent-free conditions via mechanochemistry technique. Products were obtained in excellent yields within 10 min of grinding. The reactions afforded a melt or gummy semi-solid that solidified to the desired Schiff bases within a short time. These Schiff bases were reduced to their corresponding amines, ferrocenyl-N-(pyridinylmethyl)anilines, with NaBH4 over neutral Al2 O3 solid support via grinding. Amines were obtained in excellent yields after intermittent grinding for approximately 1 h. Herein, five novel ferrocenyl-N-(pyridinylmethylene)anilines (compounds 3, 4, 6-8) and six ferrocenyl-N-(pyridinylmethyl)anilines (compounds 9-14) are reported. Compounds were characterized through FT-IR,1H-NMR, 13 C-NMR, HRMS and SC-XRD techniques. These compounds show visible solvatochromism, when UV-Vis absorption was measured in polar and nonpolar solvents. In changing solvent from polar to non-polar, the Schiff bases exhibited a blue shift while the amines portrayed a red shift. Electrochemical studies on these compounds reveal that redox behaviour of the iron centre is influenced by the position imine or amine groups. Antimicrobial properties of these compounds were studied for Escherichia coli, Staphylococcus aureus, Salmonella typhimirium and Candida albicans. Highest activity was recorded against Gram-positive bacteria and fungi.

Synthesis, characterization and cytotoxicity of some palladium(II), platinum(II), rhodium(I) and iridium(I) complexes of ferrocenylpyridine and related ligands. Crystal and molecular structure of trans-dichlorobis(3-ferrocenylpyridine)palladium(II)

Rajput, Jaisheila,Moss, John R.,Hutton, Alan T.,Hendricks, Denver T.,Arendse, Catherine E.,Imrie, Christopher

, p. 1553 - 1568 (2007/10/03)

The preparation of a series of ferrocenyl nitrogen donor ligands including ferrocenylpyridines, ferrocenylphenylpyridines and 1,1′-di(2-pyridyl)ferrocene is described. Coordination studies of the substituted pyridines (L) were carried out with platinum, palladium, rhodium and iridium. This resulted in the preparation of the following types of complexes: [MCl(CO)2(L)] and [M(cod)(L)2]ClO4 where M=Rh or Ir, cod=1,5-cyclooctadiene; [M′Cl2(L 2] where M′=Pt or Pd. The X-ray crystal structure of trans -dichlorobis(3-ferrocenylpyridine)palladium was obtained. The complexes were screened for activity against two human cancer cell lines. At least two of the complexes displayed growth inhibition similar to that of the widely used chemotherapeutic agent, cis platin.

Metallosupramolecular Cluster Assemblies based on Donor-Acceptor Type Structural Frameworks. Syntheses, Crystal Structures and Spectroscopic Properties of Novel Triosmium Alkylidyne Carbonyl Clusters bearing Remote Ferrocenyl Units as Electron Donors

Wong, Wai-Yeung,Wong, Wing-Tak,Cheung, Kung-Kai

, p. 1379 - 1388 (2007/10/02)

Two pyridyl ligands containing redox-active ferrocenyl groups 5-C5H5)(η5-C5H4C6H4R)> have been prepared using a palladium-catalysed aromatic cross-coupling reaction.Treatment of the cluster Os3(μ-

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