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81699-90-3

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81699-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81699-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,9 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81699-90:
(7*8)+(6*1)+(5*6)+(4*9)+(3*9)+(2*9)+(1*0)=173
173 % 10 = 3
So 81699-90-3 is a valid CAS Registry Number.

81699-90-3Relevant articles and documents

A General and highly efficient protocol for the synthesis of chalcogenoacetylenes by copper(I)-terpyridine catalyst

Movassagh, Barahman,Yousefi, Ali,Momeni, Badri Zaman,Heydari, Sepideh

, p. 1385 - 1390 (2014/06/23)

A highly efficient copper-catalyzed Csp-X (X = S, Se, Te) bond-forming reaction of terminal alkynes and diorganyl dichalcogenides has been developed. This transformation was realized through the use of copper(I) iodide as a catalyst, 4′-(4-meth

An efficient synthesis of alkynyl selenides and tellurides from terminal acetylenes and diorganyl diselenides or ditellurides catalyzed by recyclable copper oxide nanopowder

Godoi, Marcelo,Ricardo, Eduardo W.,Frizon, Tiago E.,Rocha, Manuela S. T.,Braga, Antonio Luiz,Singh, Devender,Paixao, Marcio W.

, p. 10426 - 10430,5 (2012/12/12)

Herein, we report an efficient method for the synthesis of alkynyl selenides and tellurides from terminal alkynes and diorganyl diselenides or ditellurides using CuO nanopowder as a recyclable catalyst. This new methodology furnished the desired products in good to excellent yields. Furthermore, the catalyst was easily recovered and reused for further catalytic reactions without loss of activity.

Short and efficient preparation of alkynyl selenides, sulfides and tellurides from terminal alkynes

Bieber, Lothar W.,Da Silva, Margarete F.,Menezes, Paulo H.

, p. 2735 - 2737 (2007/10/03)

Diphenyl diselenide reacts with terminal alkynes at room temperature in DMSO in the presence of catalytic amounts of copper iodide to give good to excellent yields of alkynyl phenyl selenides. The reaction occurs under neutral conditions and the solvent a

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