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Bis(triphenylstannyl)tellurium, with the chemical formula (C6H5)3SnTeSn(C6H5)3, is a heavy organometallic compound consisting of a central tellurium atom bonded to two triphenylstannyl groups. bis(triphenylstannyl)tellurium is characterized by its high molecular weight and complex structure, which results in unique chemical and physical properties. It is typically synthesized through the reaction of tellurium with triphenyltin chloride, and is used in various applications, including organic synthesis, as a reagent in the formation of tellurium-containing compounds, and in the study of organometallic chemistry. Due to its sensitivity to air and moisture, bis(triphenylstannyl)tellurium is usually handled under an inert atmosphere.

4324-29-2

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4324-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4324-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4324-29:
(6*4)+(5*3)+(4*2)+(3*4)+(2*2)+(1*9)=72
72 % 10 = 2
So 4324-29-2 is a valid CAS Registry Number.

4324-29-2Downstream Products

4324-29-2Relevant academic research and scientific papers

The First Phosphine-Catalyzed Insertion of Tellurium into Sn-Sn and Pb-Pb Bonds: A Simple and Efficient Route to R3MTeMR3 (M = Sn, Pb)

Han, Li-Biao,Mirzaei, Farzad,Tanaka, Masato

, p. 722 - 724 (2008/10/08)

In the presence of a catalytic amount of a phosphine, elemental tellurium efficiently inserts into Sn-Sn and Pb-Pb bonds under mild conditions to give the corresponding tellurides R3MTeMR3 (M = Sn, Pb) in quantitative yield. Mechanistic study shows that first a phosphine telluride R′3P=Te is formed via the reaction of R′3P with tellurium, which subsequently reacts with (R3M)2 to produce (R3M)2Te and concomitantly regenerates R′3P to restart another cycle of the catalytic insertion.

Synthesis, Structures and Properties of CF3S-Substituted Tellurium Compounds

Boese, Roland,Dworak, Juergen,Haas, Alois,Pryka, Michael

, p. 477 - 480 (2007/10/02)

New preparations for the following compounds are described: Te(SCF3)2, Te(NSO)2, and Cl2Te(NSO)2.The catalytic or thermal SO2 elimination from Cl2Te(NSO)2 affords a coordinated or non-coordinated thiachalcogenadiazole.Conversions of these compounds are reported.Evidence for the proposed mechanism for the reaction between Te(NSO)2 and SbCl5 is provided.Cl4Te2N2(SCF3)2, prepared from TeCl4 and CF3SN(SiMe3)2, reacts with LiN(SiMe3)2 to form 4Te2N2(SCF3)2.An X-ray structural analysis of Cl4Te2N2(SCF3)2 is presented. - Key Words: Tellurium, bis(sulfinylamido)-, bis(trifluoromethylthio)- / Thiachalcogenadiazole / Ditelluradiazetidine

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