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Dichloro(1-naphthyl)phenylsilane is an organosilicon compound with the chemical formula C18H12Cl2Si. It is a colorless to pale yellow crystalline solid that is sensitive to air and moisture. dichloro(1-naphthyl)phenylsilane is formed by the attachment of a dichlorophenyl group and a naphthyl group to a silicon atom. Dichloro(1-naphthyl)phenylsilane is primarily used as a reagent in organic synthesis, particularly in the formation of various organosilicon compounds and as a coupling agent in the synthesis of pharmaceuticals and other specialty chemicals. Due to its sensitivity to air and moisture, it is essential to handle dichloro(1-naphthyl)phenylsilane under an inert atmosphere or in a glovebox to prevent unwanted side reactions.

7751-39-5

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7751-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7751-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,5 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7751-39:
(6*7)+(5*7)+(4*5)+(3*1)+(2*3)+(1*9)=115
115 % 10 = 5
So 7751-39-5 is a valid CAS Registry Number.

7751-39-5Relevant academic research and scientific papers

Synthesis of Silacyclohexanones from Divinylsilanes and Allylamines by a Rh-Catalyzed Cyclization

Guo, Jiawei,Liu, Song,Pang, Qinjiao,Zhang, Hongyun,Gao, Lu,Chen, Li,Song, Zhenlei

supporting information, p. 726 - 730 (2022/01/20)

An efficient synthesis of silacyclohexanones bearing a variety of silyl substituents has been developed by a [Rh(coe)2Cl]2/PCy3-catalyzed cyclization of divinylsilanes with Jun’s allylamine. The silacyclohexanones can be o

Electrochemical properties of arylsilanes

Biedermann, Judith,Wilkening, H. Martin R.,Uhlig, Frank,Hanzu, Ilie

, p. 13 - 18 (2019/03/27)

In the past, the electrochemical properties of organosilicon compounds were investigated for both fundamental reasons and synthesis purposes. Little is, however, known about the electrochemical behaviour of hydrogen-bearing arylsilanes. Here, we throw light on the electrochemical properties of 11 arylsilanes compounds, 2 of them synthesized for the first time. The oxidation potentials are found to depend on both the nature and number of the aryl groups. Based on these findings it was possible to establish some variation trends that match the expected structure–property correlations. Furthermore, we present first insights into the electrochemical reaction kinetics behind and identify several soluble electrochemical oxidation products.

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