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(acetonitrile)dichloro(2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine)ruthenium(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226721-85-3

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226721-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226721-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,7,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 226721-85:
(8*2)+(7*2)+(6*6)+(5*7)+(4*2)+(3*1)+(2*8)+(1*5)=133
133 % 10 = 3
So 226721-85-3 is a valid CAS Registry Number.

226721-85-3Downstream Products

226721-85-3Relevant academic research and scientific papers

Synthesis of iron(II), manganese(II), cobalt(II) and ruthenium(II) complexes containing tridentate nitrogen ligands and their application in the catalytic oxidation of alkanes

Britovsek, George J. P.,England, Jason,Spitzmesser, Stefan K.,White, Andrew J.P.,Williams, David J.

, p. 945 - 955 (2007/10/03)

A series of Fe(II), Mn(II), Co(II) and Ru(II) complexes containing bis(imino) pyridine or bis(amino)pyridine ligands and weakly coordinating triflate (OTf-) or non-coordinating SbF6- anions have been prepared. The complexes have been fully characterized including several solid-state structure analyses. Two unusual mono-chelate six-coordinate bis(imino)pyridine Fe(II) and Mn(II) complexes have been observed. The catalytic properties of the complexes for the oxidation of cyclohexane with H2O2 have been evaluated. Only the Fe(II) complexes have shown catalytic activity, which is mainly due to Fenton-type free radical auto-oxidation. The Royal Society of Chemistry 2005.

Ruthenium(II) complexes with 2,6-pyridyl-diimine ligands: Synthesis, characterization and catalytic activity in epoxidation reactions

Cetinkaya, Bekir,Cetinkaya, Engin,Brookhart, Maurice,White, Peter S.

, p. 101 - 112 (2008/10/09)

Reaction of [RuCl2 (p-cymene)]2 with the tridentate N-N'-N ligands, 2,6-pyridyl-diimines, led to substitution of p-cymene. The resulting complexes, believed to be coordinatively unsaturated, exhibit efficient activity for the epoxidation of cyclohexene in the presence of iodosobenzene (PhIO): the complexes formed initially take up donor molecules such as acetonitrile to achieve hexacoordination. The molecular structure for one of these, (acetonitrile){2,6-bis[1-(4- methoxyphenylimino)ethyl]pyridine}dichlororuthenium(II), 2, has been determined by X-ray diffraction. The immediate coordination sphere is a distorted octahedron with trans chloride atoms and a short Ru-N(py) (1.906 A) bond.

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