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Ethanone, 2-(1-naphthalenyltelluro)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

920969-19-3

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920969-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 920969-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,0,9,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 920969-19:
(8*9)+(7*2)+(6*0)+(5*9)+(4*6)+(3*9)+(2*1)+(1*9)=193
193 % 10 = 3
So 920969-19-3 is a valid CAS Registry Number.

920969-19-3Relevant academic research and scientific papers

1-Naphthyl- and mesityltellurium(IV, II) derivatives of small bite chelating organic ligands: Effect of steric bulk and intramolecular secondary bonding interaction on molecular geometry and supramolecular association

Chauhan, Ashok K.S.,Anamika,Kumar, Arun,Srivastava, Ramesh C.,Butcher,Duthie, Andrew

, p. 5899 - 5906 (2007/10/03)

The synthesis and characterization of unsymmetric diorganotellurium compounds containing a sterically demanding 1-naphthyl or mesityl ligand and a small bite chelating organic ligand capable of 1,4-Te?N(O) intramolecular interaction is described. The reaction of ArTeCl3 (Ar = 1-C10H7, Np; 2,4,6-Me3C6H2, Mes) with (SB)HgCl [SB = the Schiff base, 2-(4,4′-NO2C6H4CH{double bond, long}NC6H3-Me)] or a methyl ketone (RCOCH3) afforded the corresponding dichlorides (SB)ArTeCl2 (Ar = Np, 1Aa; Mes, 1Ba) or (RCOCH2)ArTeCl2 (Ar = Np; R = Ph (2Aa), Me (3Aa), Np (4Aa); Ar = Mes, R = Ph (2Ba)). Reduction of 1Aa and 1Ba by Na2S2O5 readily gave the tellurides (SB)ArTe (Ar = Np (1A), Mes, (1B)) but that of dichlorides derived from methylketones was complicated due to partial decomposition to tellurium powder and diarylditelluride (Ar2Te2), resulting in poor yields of the corresponding tellurides 2A, 2B and 3A. Oxidation of the isolated tellurides with SO2Cl2, Br2 and I2 yielded the corresponding dihalides. All the synthesized compounds have been characterized with the help of IR, 1H, 13C, and 125Te NMR and in the case of 2Aa, and 2Ba by X-ray crystallography. Appearance of only one 125Te signal indicated that the unsymmetric derivatives were stable to disproportionation to symmetric species. Intramolecular 1,4-Te?O secondary bonding interactions (SBIs) are exhibited in the crystal structures of both the tellurium(IV) dichlorides, 2Aa, and 2Ba. Steric repulsion of the mesityl group in the latter dominates over lone pair-bond pair repulsion, resulting in significant widening of the equatorial C-Te-C angle. This appears to be responsible for the lack of Te?Cl involved supramolecular associations in the crystal structure of 2Ba.

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