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

28192-35-0

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28192-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28192-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,9 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28192-35:
(7*2)+(6*8)+(5*1)+(4*9)+(3*2)+(2*3)+(1*5)=120
120 % 10 = 0
So 28192-35-0 is a valid CAS Registry Number.

28192-35-0Relevant academic research and scientific papers

Pentafluoro(aryl)-λ6-tellanes and Tetrafluoro(aryl)(trifluoromethyl)-λ6-tellanes: From SF5 to the TeF5 and TeF4CF3 Groups

Bornemann, Dustin,Pitts, Cody Ross,Ziegler, Carmen J.,Pietrasiak, Ewa,Trapp, Nils,Kueng, Sebastian,Santschi, Nico,Togni, Antonio

supporting information, p. 12604 - 12608 (2019/08/16)

The TeF5 group is significantly underexplored as a highly fluorinated substituent on an organic framework, despite it being a larger congener of the acclaimed SF5 group. In fact, only one aryl-TeF5 compound (phenyl-TeFsub

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 (2013/09/02)

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.

Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes

Singh, Fateh V.,Stefani, Hélio A.

experimental part, p. 863 - 867 (2010/03/24)

An ultrasound-assisted synthesis of functionalized symmetrical biaryls with electron-withdrawing or electron-donating substituents is described and illustrated by the palladium-catalyzed detelluration of 1,2-diarylditellanes. This procedure offers easy access to symmetrical biaryls in short reaction time and the products are achieved in good to excellent yields.

Direct Synthesis of Some Diaryl Ditellurides from Aryl Halides

Liu, Jianfei,Qiu, Mei,Zhou, Xunjun

, p. 2759 - 2767 (2007/10/02)

The reaction of aryl halides with sodium hydrogen telluride in dimethylformamide is studied.Some diaryl ditellurides are synthesized under mild conditions by the reaction.

Improved preparation of diaryl ditellurides

Engman, Lars,Persson, Joachim

, p. 71 - 74 (2007/10/02)

Diaryl ditellurides have been synthesized from aryl bromides via lithiation, tellurium insertion, and ferricyanide oxidation of the resulting lithium arenetellurolates.

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