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898289-50-4

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898289-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898289-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,8 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 898289-50:
(8*8)+(7*9)+(6*8)+(5*2)+(4*8)+(3*9)+(2*5)+(1*0)=254
254 % 10 = 4
So 898289-50-4 is a valid CAS Registry Number.

898289-50-4Downstream Products

898289-50-4Relevant articles and documents

Cyclometallated 2-Phenylpyrimidine Derived Platinum Complexes: Synthesis and Photophysical Properties

Fecková, Michaela,Kahlal, Samia,Roisnel, Thierry,Saillard, Jean-Yves,Boixel, Julien,Hruzd, Mariia,le Poul, Pascal,Gauthier, Sébastien,Robin-le Guen, Fran?oise,Bure?, Filip,Achelle, Sylvain

, p. 1592 - 1600 (2021/04/28)

A series of five platinum (II) complexes based on 2-phenylpyrimidine ligands have been designed. Pyridine and chloride were used as auxiliary ligands. These complexes exhibit a slightly distorted square-planar geometry. The nature and position of substitu

Ruthenium-Catalyzed meta-Selective CAr-H Bond Formylation of Arenes

Jia, Chunqi,Wu, Nini,Cai, Xiaofeng,Li, Gang,Zhong, Lei,Zou, Lei,Cui, Xiuling

, p. 4536 - 4542 (2020/04/09)

The meta-CAr-H bond formylation of arenes has been achieved using CHBr3 as a formyl source in the presence of [Ru(p-cym)(OAc)2] as a catalyst. This method provides efficient access to the preparation of various meta-substituted aromatic compounds, such as alcohols, ethers, amines, nitriles, alkenes, halogens, carboxylic acids, and their derivatives, through transformation of the versatile formyl group. Furthermore, mechanistic studies show that the key active species is a pentagonal ruthenacycle complex.

"Nanorust"-catalyzed benign oxidation of amines for selective synthesis of nitriles

Jagadeesh, Rajenahally V.,Junge, Henrik,Beller, Matthias

, p. 92 - 96 (2015/02/19)

Organic nitriles constitute key precursors and central intermediates in organic synthesis. In addition, nitriles represent a versatile motif found in numerous medicinally and biologically important compounds. Generally, these nitriles are synthesized by traditional cyanation procedures using toxic cyanides. Herein, we report the selective and environmentally benign oxidative conversion of primary amines for the synthesis of structurally diverse aromatic, aliphatic and heterocyclic nitriles using a reusable "nanorust" (nanoscale Fe2O3)-based catalysts applying molecular oxygen.

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