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C23H22CuN3O2(1+)*NO3(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1569104-93-3

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1569104-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569104-93-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,1,0 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1569104-93:
(9*1)+(8*5)+(7*6)+(6*9)+(5*1)+(4*0)+(3*4)+(2*9)+(1*3)=183
183 % 10 = 3
So 1569104-93-3 is a valid CAS Registry Number.

1569104-93-3Upstream product

1569104-93-3Downstream Products

1569104-93-3Relevant academic research and scientific papers

Synthesis and characterization of copper(ii) 4′-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols

Ma, Zhen,Wei, Lijuan,Alegria, Elisabete C.B.A.,Martins, Luisa M.D.R.S.,Guedes Da Silva, M. Fatima C.,Pombeiro, Armando J.L.

, p. 4048 - 4058 (2014)

The reactions between 4′-phenyl-terpyridine (L) and nitrate, acetate or chloride Cu(ii) salts led to the formation of [Cu(NO3) 2L] (1), [Cu(OCOCH3)2L]·CH 2Cl2 (2·CH2Cl2) and [CuCl2L]·[Cu(Cl)(μ-Cl)L]2 (3), respectively. Upon dissolving 1 in mixtures of DMSO-MeOH or EtOH-DMF the compounds [Cu(H 2O){OS(CH3)2}L](NO3)2 (4) and [Cu(HO)(CH3CH2OH)L](NO3) (5) were obtained, in this order. Reaction of 3 with AgSO3CF3 led to [CuCl(OSO2CF3)L] (6). The compounds were characterized by ESI-MS, IR, elemental analysis, electrochemical techniques and, for 2-6, also by single crystal X-ray diffraction. They undergo, by cyclic voltammetry, two single-electron irreversible reductions assigned to Cu(ii) → Cu(i) and Cu(i) → Cu(0) and, for those of the same structural type, the reduction potential appears to correlate with the summation of the values of the Lever electrochemical EL ligand parameter, which is reported for the first time for copper complexes. Complexes 1-6 in combination with TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxyl radical) can exhibit a high catalytic activity, under mild conditions and in alkaline aqueous solution, for the aerobic oxidation of benzylic alcohols. Molar yields up to 94% (based on the alcohol) with TON values up to 320 were achieved after 22 h.

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