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(4-chlorophenyl)(phenylethynyl)tellane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59130-72-2

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59130-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59130-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59130-72:
(7*5)+(6*9)+(5*1)+(4*3)+(3*0)+(2*7)+(1*2)=122
122 % 10 = 2
So 59130-72-2 is a valid CAS Registry Number.

59130-72-2Downstream Products

59130-72-2Relevant academic research and scientific papers

Magnetite (Fe3O4) nanoparticles: An efficient and recoverable catalyst for the synthesis of alkynyl chalcogenides (selenides and tellurides) from terminal acetylenes and diorganyl dichalcogenides

Godoi, Marcelo,Liz, Daiane G.,Ricardo, Eduardo W.,Rocha, Manuela S.T.,Azeredo, Juliano B.,Braga, Antonio L.

, p. 3349 - 3354 (2014)

We present herein a new and efficient methodology for the synthesis of alkynyl chalcogenides from terminal acetylenes and diorganyl dichalcogenides, catalyzed by Fe3O4 nanoparticles. This new approach provided the desired products in good to excellent yields. Moreover, the catalyst was easily recoverable using an external magnet and reused for further experiments without loss of catalytic activity.

Synthesis of alkynyltellurides mediated by K3PO4 and DMSO

Do Sacramento, Manoela,Menezes, Larissa,Goldani, Bruna,Perin, Gelson,Silva, Marcio S.,Barcellos, Thiago,Alves, Diego

supporting information, p. 11091 - 11098 (2019/07/31)

In the present work, a simple method for the synthesis of alkynyltellurides is described by the reactions of terminal alkynes with diorganyl ditellurides in the presence of a catalytic amount of K3PO4. In both substrates, it was possible to vary the aryl and alkyl groups, obtaining the products of interest in short reaction times and in yields ranging from 30 to 93%. This methodology, different from those already reported in the literature, has the advantage of using a catalytic amount of a weak base and no use of metallic catalysts.

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