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(1-na)3SiH, also known as tri(1-naphthyl)silane, is a silane compound with the chemical formula C36H27Si. It contains three 1-naphthyl groups, which are aromatic hydrocarbons derived from naphthalene. (1-na)3SiH is known for its high thermal stability and ability to form stable bonds with other materials, making it a valuable component in various electronic and optoelectronic devices.

2536-76-7

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2536-76-7 Usage

Uses

Used in Organic Light-Emitting Diodes (OLEDs):
(1-na)3SiH is used as a photoconductor in OLEDs for its ability to improve the performance and efficiency of these devices.
Used in Perovskite Solar Cells:
In the photovoltaic industry, (1-na)3SiH serves as a hole-transport material in perovskite solar cells, enhancing their overall efficiency and stability.
Used in Organic Semiconductors:
(1-na)3SiH has potential applications in the development of organic semiconductors, where its properties can contribute to the advancement of electronic and optoelectronic technologies.
Used as a Building Block in Organic Synthesis:
Tri(1-naphthyl)silane can also be utilized as a building block in the synthesis of more complex organic compounds, further expanding its applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 2536-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2536-76:
(6*2)+(5*5)+(4*3)+(3*6)+(2*7)+(1*6)=87
87 % 10 = 7
So 2536-76-7 is a valid CAS Registry Number.

2536-76-7Relevant academic research and scientific papers

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.

INTRAMOLECULAR PRINS REACTION AND CATALYSTS SUITABLE THEREFOR

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Page/Page column 34-35, (2008/06/13)

The present invention relates to a process for the preparation of a compound of the formula B having the following steps: provision of a compound of the formula A intramolecular reaction of the compound of the formula A in the presence of an aluminium siloxide of the formula (Ia) or (Ib).

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