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Di-p-biphenyltin dihydride, also known as diphenyltin dihydride, is an organotin compound with the chemical formula (C6H5)2SnH2. It is a colorless, crystalline solid that is sensitive to air and moisture. di-p-biphenyltin dihydride is formed by the reaction of diphenyltin oxide with hydrogen gas in the presence of a catalyst, such as triethylsilane. Di-p-biphenyltin dihydride is an important intermediate in the synthesis of various organotin compounds, which have applications in the fields of polymer chemistry, catalysis, and as biocides in antifouling paints. Due to its sensitivity to air and moisture, it is typically handled under an inert atmosphere or in a glovebox.

1050-07-3

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1050-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1050-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1050-07:
(6*1)+(5*0)+(4*5)+(3*0)+(2*0)+(1*7)=33
33 % 10 = 3
So 1050-07-3 is a valid CAS Registry Number.

1050-07-3Downstream Products

1050-07-3Relevant academic research and scientific papers

Aryltin chlorides and hydrides: Preparation, detailed NMR studies and DFT calculations

Zeppek, Cathrin,Pichler, Johann,Torvisco, Ana,Flock, Michaela,Uhlig, Frank

supporting information, p. 41 - 49 (2013/10/01)

A series of novel tin chlorides RnSnCl4-n and respective hydrides RnSnH4-n were synthesized displaying a range of substituted phenyl residues, as well as naphthyl moieties (R = Ph, o-tolyl, 2,4-xylyl, 2,6-xylyl, p-biphenyl, 1-naphthyl, 2-naphthyl). These compounds were characterized using 1H, 13C and 119Sn NMR spectroscopy. In addition, X-ray diffraction was employed to elucidate the molecular structure of all solid aryltin chlorides (8e10, 14, 15). In each case, the tin is in a distorted tetrahedral environment. All naphthyl containing derivatives exhibit displaced π-π stacking. DFT calculations were carried out to compare experimental NMR data with calculated 13C and 119Sn shifts, as well as 13C-119Sn coupling constants.

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