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Tris(cyclohexyl)(phenyl)stannane, also known as tricyclohexylphenylstannane, is an organotin compound with the chemical formula C18H31Sn. It is a colorless, viscous liquid that is soluble in organic solvents. tris(cyclohexyl)(phenyl)stannane is primarily used as a catalyst in various chemical reactions, including the production of polyurethane foams and the synthesis of organotin compounds. It is also employed as a stabilizer for PVC and as a heat stabilizer for polyolefins. Due to its potential environmental and health risks, the use of tris(cyclohexyl)(phenyl)stannane is subject to regulations in some regions.

20204-08-4

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20204-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20204-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20204-08:
(7*2)+(6*0)+(5*2)+(4*0)+(3*4)+(2*0)+(1*8)=44
44 % 10 = 4
So 20204-08-4 is a valid CAS Registry Number.

20204-08-4Relevant academic research and scientific papers

Synthesis of arylstannanes by palladium-catalyzed desulfitative coupling reaction of sodium arylsulfinates with distannanes

Lian, Chang,Yue, Guanglu,Zhang, Haonan,Wei, Liyan,Liu, Danyang,Liu, Sichen,Fang, Huayi,Qiu, Di

supporting information, p. 4019 - 4023 (2018/10/04)

A novel Pd-catalyzed desulfitative cross-coupling reaction of sodium arylsulfinates with hexaalkyl distannanes is realized, allowing the facile synthesis of functionalized arylstannanes with moderate to excellent yields. The successful implement of gram-scale synthesis and tandem Stille coupling reaction demonstrates the potential applications of this method in organic synthesis.

RECYCLING OF ORGANOTIN COMPOUNDS

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Page/Page column 28; 35, (2013/12/03)

A method for the synthesis of a first organic molecule, said method comprising the steps of: a) Reacting a first reactant with an organotin reactant having at least one optionally substituted organic group having from 5 to 20 carbon atoms selected from alkyl, alkenyl, alkynyl, alkoxyalkyl, alkoxy, alkylthioalkyl, carboxylates and alkylaminoalkyl groups, thereby forming a mixture of a product and a tin-containing by-product, and b) Removing most of the tin-containing by-product from said mixture in such a way as to provide a purified product comprising less than 1000 ppm of remaining tin-containing by- product, wherein said step of removing most of said tin-containing by-product is either an extraction between a first liquid and a second liquid, said second liquid being more polar than said first liquid and at least partly immiscible therewith or is a reversed phase chromatography.

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