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Triphenyltelluronium chloride, with the chemical formula (C6H5)3TeCl, is a compound consisting of a tellurium atom bonded to three phenyl groups and a chloride ion. It is a white crystalline solid that is soluble in organic solvents such as chloroform and dichloromethane. This organotellurium compound is used as a reagent in organic synthesis, particularly in the formation of carbon-tellurium bonds and as a precursor for the synthesis of other tellurium-containing compounds. It is also known for its potential applications in materials science and as a catalyst in certain chemical reactions. Triphenyltelluronium chloride is typically handled with care due to its sensitivity to air and moisture, and it is stored under an inert atmosphere to prevent decomposition.

1224-13-1

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1224-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1224-13:
(6*1)+(5*2)+(4*2)+(3*4)+(2*1)+(1*3)=41
41 % 10 = 1
So 1224-13-1 is a valid CAS Registry Number.

1224-13-1Upstream product

1224-13-1Relevant academic research and scientific papers

THE REACTIONS OF SELENIUM TETRACHLORIDE AND TELLURIUM TETRACHLORIDE WITH SOME TRIVALENT ARYL ORGANOMETALLIC HALIDES

Rainville, David P.,Zingaro, Ralph A.

, p. 277 - 288 (1980)

The reactions of several trivalent organometallic aryl compounds with TeCl4 and SeCl4 were investigated.When diphenylboron bromide was treated with an equimolar quantity of tellurium tetrachloride in toluene, the phenyltellurium trihalide C6H5TeBr1.3Cl1.7 was obtained.The presence of the mixed halogens on tellurium can be explained in terms of a Lewis acid-base reaction between the boron and tellurium compounds.The reaction of diphenylboron bromide with selenium tetrachloride in toluene, produced mixed triarylselenonium chlorides.The presence of substituted toluenemolecules in the product is attributed to the reaction of selenium tetrachloride with toluene in the presence of the Lewis acid, boron trihalide.The reaction of triphenylaluminum with tellurium tetrachloride was found to produce triphenyl telluronium chloride.Both diphenylchloroarsine and diphenylchlorophosphine were oxidized from MIII to MV by either selenium or tellurium tetrachloride.The products were isolated as diphenylarsinic acid and diphenylphosphinic acid, respectively.

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