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The chemical compound "(C4H9)3SnOC(C6H5)2" is a triorganotin compound, specifically a trialkyltin derivative. It consists of a central tin (Sn) atom bonded to three butyl groups (C4H9) and a single phenoxide group (OC(C6H5)2), where the phenoxide group is derived from diphenyl ether. (C4H9)3SnOC(C6H5)2 is known for its potential applications as a catalyst, a stabilizer for polymers, and in the production of certain types of plastics. It is also recognized for its biocidal properties, which have led to its use as a pesticide, although its environmental impact and toxicity have raised concerns, leading to restrictions on its use in some regions. The compound's structure and properties make it a subject of interest in organometallic chemistry and materials science.

68825-74-1

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68825-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68825-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68825-74:
(7*6)+(6*8)+(5*8)+(4*2)+(3*5)+(2*7)+(1*4)=171
171 % 10 = 1
So 68825-74-1 is a valid CAS Registry Number.

68825-74-1Downstream Products

68825-74-1Relevant academic research and scientific papers

O,O'-Bistributyltin Benzopinacolate (1,1,2,2-Tetraphenylethane-1,2-bisolate) as Thermal Source of Tributylstannyl Radicals

Tomaszewski, Miroslaw J.,Warkentin, John

, p. 1407 - 1408 (2007/10/02)

The previously unknown bistributyltin benzopinacolate was prepared by photolysis of benzophenone in the presence of bistributyltin and used for thermal formation of aryl radicals that undergo subsequent intramolecular addition to an imine bond in an ortho-substituent.

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