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Triphenyltin p-methoxyphenyl mercaptide is an organotin compound characterized by the presence of a triphenyltin group and a p-methoxyphenyl mercaptide group. It is a colorless, crystalline solid with the chemical formula C25H21OSn. triphenyltin p-methoxyphenyl mercaptide is formed by the reaction of triphenyltin chloride with p-methoxyphenyl mercaptan, resulting in a product with potential applications in various fields, such as agriculture and materials science. Triphenyltin p-methoxyphenyl mercaptide exhibits unique chemical properties, including its ability to act as a fungicide and its potential use in the synthesis of other organotin compounds. Due to its organotin nature, it is essential to handle triphenyltin p-methoxyphenyl mercaptide with care, as organotin compounds can be toxic to both humans and the environment.

55216-02-9

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55216-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55216-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,1 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55216-02:
(7*5)+(6*5)+(5*2)+(4*1)+(3*6)+(2*0)+(1*2)=99
99 % 10 = 9
So 55216-02-9 is a valid CAS Registry Number.

55216-02-9Downstream Products

55216-02-9Relevant academic research and scientific papers

REACTIONS OF TETRAPHENYLANTIMONY MERCAPTIDES

Wardell, James L.,Grant, Douglas W.

, p. 121 - 130 (1980)

Reactions of tetraphenylantimony mercaptides, Ph4SbSC6H4Y, with electrophilic species in chlorocarbon solutions are reported.With chloromethyl methyl sulphide, allyl halides, sulphenyl halide, acyl halides, halogens, and triphenyltin chloride, ready and complete halide-mercaptide exchanges occur.No allylic rearrangement is found in the reaction with trans-PhCH=CHCH2Br.In a competition reaction for ClCH2SMe, Ph4SbSC6H5 was shown to be only slightly (ca. 1.2 times) more reactive than Ph4SbSC6H4OMe-p.The initial sulphur-containing product of reaction with p-toluenesulphonyl chloride, namely the thiosulphonate, p-MeC6H4SO2SC6H4Y, reacts further with Ph4SbSC6H4Y to produce the disulphide, (YC6H4S)2.Benzoyl peroxide and Ph4SbSC6H4 provide PhSbOCOPh and disulphide.

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