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triphenyltin 4-methylbenzenecarbothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220947-39-7

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220947-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220947-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,9,4 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220947-39:
(8*2)+(7*2)+(6*0)+(5*9)+(4*4)+(3*7)+(2*3)+(1*9)=127
127 % 10 = 7
So 220947-39-7 is a valid CAS Registry Number.

220947-39-7Downstream Products

220947-39-7Relevant academic research and scientific papers

Facile synthesis and structure of heavy alkali metal thiocarboxylates: Structural comparison with the selenium and tellurium isologues

Niyomura, Osamu,Kato, Shinzi,Kanda, Takahiro

, p. 507 - 518 (2008/10/08)

Potassium, rubidium, and cesium thiocarboxylates were found to be synthesized by the reaction of thiocarboxylic acid or its O-trimethylsilyl esters with KF, RbF, and CsF. Tetramethylammonium thiocarboxylates were prepared in good yields by the reaction of sodium thiocarboxylates with tetramethylammonium chloride. The structures of potassium benzene-, 2-methoxybenzene-, and 4-methoxybenzenecarbothioates, rubidium 2-methoxybenzenecarbothioate, tetramethylammonium 2-methoxy- and 2-trifiuoromethylbenzenecarbothioates, potassium 2-methoxybenzenecarboselenoate, and rubidium 2-methoxybenzenecarbotelluroate were characterized by X-ray structural analysis. All of these alkali metal salts exhibit a dimeric structure in which the oxygen and/or sulfur atom is associated with the metal of the opposite molecule, while the tetramethylammonium thiocarboxylates are monomeric. In potassium 2-methoxybenzenecarbothioate, the two thiocarboxylate groups chelate to the potassium atoms above and below the plane which involves the thiocarboxylate groups. In potassium 4-methoxybenzenecarbothioate, one thiocarboxylate group chelates to potassium. Without exception, the o-methoxy oxygen intermolecularly coordinates to the metal of the opposite molecule. The C-O bond lengths of the thiocarboxylate group are in the range 1.22-1.24 A, which is slightly longer than those of common thioesters. The C(sp2)-S distances are in the range 1.70-1.72 A, which is close to that of a typical C-S single bond and suggests that the negative charge may be somewhat localized on the sulfur atom. The interaction number of the metals with oxygen and sulfur atoms was 7 for K and 8 for both Rb and Cs. The dihedral angle between the thiocarboxyl group and the phenyl ring is substantially increased by the introduction of the o-methoxy group. In these alkali metal thio-, seleno-, and tellurocarboxylates, only cesium 2-methoxybenzenecarbotelluroate showed an intermolecular nonbonding interaction between the cesium and the phenyl ring carbons.

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