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bis(4-nitrophenyl) ditelluride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132387-68-9

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132387-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132387-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132387-68:
(8*1)+(7*3)+(6*2)+(5*3)+(4*8)+(3*7)+(2*6)+(1*8)=129
129 % 10 = 9
So 132387-68-9 is a valid CAS Registry Number.

132387-68-9Upstream product

132387-68-9Downstream Products

132387-68-9Relevant academic research and scientific papers

Iron-catalyzed formation of C-Se and C-Te bonds through cross coupling of aryl halides with Se(0) and Te(0)/nano-Fe3O4@GO

Kassaee, Mohammadzaman,Motamedi, Elaheh,Movassagh, Barahman,Poursadeghi, Samira

, p. 2337 - 2342 (2013)

The formation of C-Se and C-Te bonds is of synthetic and biological importance. Graphene oxide based nano-Fe3O4 (nano-Fe 3O4@GO) is used as a reusable catalyst for the efficient synthesis of diselenides and ditellurides, through cross coupling of Se(0) or Te(0) with aryl iodides. The magnetic heterogeneous catalyst could be easily recovered and reused many times without significant loss of catalytic activity. In addition the superiority of nano-Fe3O4@GO over pristine nano-Fe3O4 is established. Georg Thieme Verlag Stuttgart. New York.

Microwave-assisted one-pot synthesis of symmetrical diselenides, ditellurides and disulfides from organoyl iodides and elemental chalcogen catalyzed by CuO nanoparticles

Botteselle, Giancarlo V.,Godoi, Marcelo,Galetto, Fabio Z.,Bettanin, Luana,Singh, Devender,Rodrigues, Oscar E.D.,Braga, Antonio L.

, p. 186 - 193 (2013/01/14)

In this study CuO nanoparticles were applied as a catalyst for CSe, CTe, and CS bond formation. The reaction was performed with organoyl iodides and elemental selenium, tellurium or sulfur under microwave irradiation in the presence of a base and solvent at 80 °C. This novel protocol allowed the synthesis of a variety of diselenides, ditellurides and disulfides in good to excellent yields in a very short reaction time.

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