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bis[(2-(phenylazo)phenyl-C,N')tellurium]oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1263181-83-4

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1263181-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263181-83-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,1,8 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1263181-83:
(9*1)+(8*2)+(7*6)+(6*3)+(5*1)+(4*8)+(3*1)+(2*8)+(1*3)=144
144 % 10 = 4
So 1263181-83-4 is a valid CAS Registry Number.

1263181-83-4Downstream Products

1263181-83-4Relevant academic research and scientific papers

Isolation and structural characterization of some aryltellurium halides and their hydrolyzed products stabilized by an intramolecular Te...N interaction

Srivastava, Kriti,Shah, Poonam,Singh, Harkesh B.,Butcher, Ray J.

experimental part, p. 534 - 546 (2011/03/21)

The isolation of pure [2-(phenylazo)phenyl-C,N′]tellurium(IV) tribromide (6) has been achieved by modifying the reported procedure, which involved transmetalation of [2-(phenylazo)phenyl-C,N′]mercury(II) chloride (7) with TeBr4. The mixed-valent derivative bis[2-(phenylazo)phenyl- C,N′]ditellurium dichloride (19), incorporating both a divalent and a tetravalent tellurium, was obtained serendipitously during the reduction of [2-(phenylazo)phenyl-C,N′]tellurium(IV) trichloride (16) with hydrazine hydrate. Bis[2-(phenylazo)phenyl-C,N′]telluride (10) has been synthesized by the ortho-lithiation route. Telluride 10, on treatment with SO 2Cl2 and Br2, underwent oxidative addition to give the expected Te(IV) halogenated products bis[2-(phenylazo)phenyl-C, N′]tellurium(IV) dichloride (13) and bis[2-(phenylazo)phenyl-C,N′] tellurium(IV) dibromide (11), respectively. However, a similar reaction of 10 with I2 resulted in the formation of an unexpected telluronium cation, iodobis[2-(phenylazo)phenyl-C,N′]telluronium triiodide (14), and [2-(phenylazo)phenyl-C,N′]tellurenenyl(II) iodide (12). Alkaline hydrolysis of 16 under reflux conditions resulted in the formation of monomeric [2-(phenylazo)phenyl-C,N′]tellurinic acid (20) and its sodium salt (21) as a cocrystal. Bis[[2-(phenylazo)phenyl-C,N′]tellurium]oxide (22) was obtained from the hydrolysis of [2-(phenylazo)phenyl-C,N′]tellurium(II) chloride (17). The reaction of 13 with an alkaline solution resulted in the formation of the corresponding bis[2-(phenylazo)phenyl-C,N′]tellurium(IV) oxide (23) and dichlorobis[2-(phenylazo)phenyl-C,N′]tellurium(IV) oxide (24). The identity of all the derivatives was confirmed by multinuclear NMR (1H, 13C, 125Te) and FT-IR spectroscopy, elemental analysis, and ESI-MS. The structures for tellurium derivatives 6, 10-14, 17, 19, 20-23, and 23A were also confirmed by X-ray crystallography. Density functional theory (DFT) was utilized for optimizing the geometries of 11, 13, and 14 to examine the possibility of a four-membered intramolecular Te...N interaction.

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