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(3,5-(CF3)2C6H3NH0.5C(CF3))2CH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

628301-50-8

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628301-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 628301-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 628301-50:
(8*6)+(7*2)+(6*8)+(5*3)+(4*0)+(3*1)+(2*5)+(1*0)=138
138 % 10 = 8
So 628301-50-8 is a valid CAS Registry Number.

628301-50-8Relevant academic research and scientific papers

Modulating the steric, electronic, and catalytic properties of Cp* ruthenium half-sandwich complexes with β-diketiminato ligands

Phillips, Andrew D.,Thommes, Katrin,Scopelliti, Rosario,Gandolfi, Claudio,Albrecht, Martin,Severin, Kay,Schreiber, Dominique F.,Dyson, Paul J.

, p. 6119 - 6132 (2011)

Five different types of β-diketiminate ligands, bearing electron-donating to strongly electron-withdrawing substituents, were synthesized and used in the synthesis of Cp* ruthenium complexes (Cp* = η5-C5Me5). One series consists of complexes with a covalent RuIII-Cl bond, and the other series features a reduced RuII center, where the chloride is abstracted by treatment of the corresponding RuIII compounds with Zn or Mg. All compounds were characterized by single-crystal X-ray diffraction, UV-visible spectroscopy, and cyclic voltammetry. In the case of RuII complexes, solution NMR techniques provided key information regarding the electronic and structural differences induced by the different β-diketiminate ligands employed. Capitalizing on the facile reduction-oxidation cycle of the Cp* ruthenium β-diketiminato complexes, catalytic atom transfer radical addition (ATRA) and cyclization (ATRC) reactions were performed on relevant substrates. The turnover rates are strongly dependent on the type of β-diketiminate used, where ligands with electron-withdrawing substituents, i.e., trifluoromethyl groups, provided complexes that efficiently catalyze the addition of CCl4 or toluenesulfonyl chloride to styrene. In contrast, complexes with electron-donating substituents on the β-diketiminate promoted efficient ATR cyclization of N-allyl-N-phenyltrichloroacetamide and 2,2,2-trichloroethyl ether. Thus, the overall product conversion and yield are dependent on matching the ligand substitution pattern of the catalyst to the type of substrate.

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