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tetrakis[4-(3-thiophenyl)phenyl]methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1287732-71-1

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1287732-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1287732-71-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1287732-71:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*3)+(3*2)+(2*7)+(1*1)=191
191 % 10 = 1
So 1287732-71-1 is a valid CAS Registry Number.

1287732-71-1Downstream Products

1287732-71-1Relevant academic research and scientific papers

Tetraphenylmethane or silane-based compound as well as preparation method and application thereof

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Paragraph 0056; 0057; 0065, (2017/10/09)

The invention provides a tetraphenylmethane or silane-based compound shown in formula (I), a preparation method of the tetraphenylmethane or silane-based compound and application of the tetraphenylmethane or silane-based compound in synthesizing an electrochromic material membrane as a monomer. As the tetraphenylmethane or silane-based compound has a space structure of tetrahedral tetrad, through membrane formation with electrochemcial polymerization, the obtained membrane expresses larger specific surface area and good electrochemical performance such as electrochromism and the like at the same time. The contrast of the membrane is 30-80 percent, the response time of the membrane is between 0.5s and 6s, the contrast and the response time both express reasonable electrochemcial stable activity, and experimental results show that the material is a potential electrochromic material. The formula of the tetraphenylmethane or silane-based compound is shown in the description.

Fourfold Suzuki-Miyaura and Sonogashira cross-coupling reactions on tetrahedral methane and adamantane derivatives

Schilling, Christine I.,Plietzsch, Oliver,Nieger, Martin,Muller, Thierry,Braese, Stefan

experimental part, p. 1743 - 1754 (2011/05/05)

An efficient way to generate a series of rigid tetrahedral organic building units from common methane and adamantane precursors is presented. Suzuki-Miyaura and Sonogashira cross-coupling reactions are used to effectively generate these shape-persistent m

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