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93453-80-6

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93453-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93453-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93453-80:
(7*9)+(6*3)+(5*4)+(4*5)+(3*3)+(2*8)+(1*0)=146
146 % 10 = 6
So 93453-80-6 is a valid CAS Registry Number.

93453-80-6Relevant articles and documents

Highly efficient homogeneous and heterogenized ruthenium catalysts for transfer hydrogenation of carbonyl compounds

Ganesamoorthy,Jerome,Shanmugasundaram,Karvembu

, p. 27955 - 27962 (2014)

[Ru(acac)2(CH3CN)2] was synthesized from [Ru(acac)3] by refluxing it with zinc powder in ethanol-acetonitrile mixture. The prepared catalyst was characterized by FT-IR, 1H and 13C NMR techniques. The silica supported catalyst ('SiO 2'-NH2-RuII) was prepared by stirring [Ru(acac)2(CH3CN)2] with 'SiO 2'-NH2 in a 1:1 mixture of CH2Cl 2-toluene for 3 days at room temperature. It was characterized by FT-IR, SEM, solid state NMR, ICP and BET surface area methods. The transfer hydrogenation reaction of carbonyl compounds was carried out separately using [Ru(acac)2(CH3CN)2] and 'SiO 2'-NH2-RuII as catalysts. The reaction conditions were optimized with different solvents, bases, catalyst amounts and temperatures using acetophenone as a model system. The scope of the reaction was extended to various substituted aryl ketones including heteroaryl ketones. This journal is the Partner Organisations 2014.

Rhodium nanoparticles supported on 2-(aminomethyl)phenols-modified Fe3O4 spheres as a magnetically recoverable catalyst for reduction of nitroarenes and the degradation of dyes in water

Chen, Tian,Chen, Zhangpei,Hu, Jianshe,Lv, Kexin,Reheman, Aikebaier,Wang, Gongshu

, (2021/06/18)

A magnetic nanostructured catalyst (Fe3O4@SiO2-Amp-Rh) modified with 2-(aminomethyl)phenols (Amp) was designed and prepared, which is used to catalyze the reduction of aromatic nitro compounds into corresponding amines and the degradation of dyes. The 2-aminomethylphenol motif plays a vital role in the immobilization of rhodium nanoparticles to offer extraordinary stability, which has been characterized by using various techniques, including transmission electron microscopy (TEM), thermal gravimetric analyzer (TGA), X-Ray Diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). A variety of nitroaromatic derivatives have been reduced to the corresponding anilines in water with up to yields of 99% within 1?h at room temperature. In addition, the catalyst system is effective in catalyzing the reduction of toxic pollutant 4-nitrophenol and the degradation of MO, MB and RhB dyes. Importantly, this catalyst Fe3O4@SiO2-Amp-Rh can be easily recovered by an external magnetic field because of the presence of magnetic core of Fe3O4, and the activity of Fe3O4@SiO2-Amp-Rh does not decrease significantly after 7 times’ recycling, which indicates that the catalyst performed high reactivity as well as stability. Graphical abstract: [Figure not available: see fulltext.]

Chemoselective reduction of nitroarenes, N-acetylation of arylamines, and one-pot reductive acetylation of nitroarenes using carbon-supported palladium catalytic system in water

Zeynizadeh, Behzad,Mohammad Aminzadeh, Farkhondeh,Mousavi, Hossein

, p. 3289 - 3312 (2021/05/11)

Developing and/or modifying fundamental chemical reactions using chemical industry-favorite heterogeneous recoverable catalytic systems in the water solvent is very important. In this paper, we developed convenient, green, and efficient approaches for the chemoselective reduction of nitroarenes, N-acetylation of arylamines, and one-pot reductive acetylation of nitroarenes in the presence of the recoverable heterogeneous carbon-supported palladium (Pd/C) catalytic system in water. The utilize of the simple, effective, and recoverable catalyst and also using of water as an entirely green solvent along with relatively short reaction times and good-to-excellent yields of the desired products are some of the noticeable features of the presented synthetic protocols. Graphic abstract: [Figure not available: see fulltext.].

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