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1,4-Benzenediselenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36987-10-7

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36987-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36987-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,8 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36987-10:
(7*3)+(6*6)+(5*9)+(4*8)+(3*7)+(2*1)+(1*0)=157
157 % 10 = 7
So 36987-10-7 is a valid CAS Registry Number.

36987-10-7Relevant academic research and scientific papers

Reversibly thermochromic bismuth-organic materials with tunable optical gaps

Zhang, Guoxian,Chan, Julian M. W.

, p. 10007 - 10015 (2017/10/13)

Five reversibly thermochromic bismuth-based inorganic-organic hybrid materials were synthesized via facile one-step condensation reactions between triphenylbismuth and four arenedithiols and a diselenol. The materials were characterized by UV-vis and FT-IR spectroscopy, powder X-ray diffraction (PXRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), elemental analysis (EA), and thermogravimetric analysis (TGA). The bismuth-organic materials (Bi-OMs) are colored materials with optical HOMO-LUMO gaps that were readily tuned by systematic modification of the steric and electronic character of the π-conjugated organic linkers. All five Bi-OMs exhibit completely reversible thermochromism in the solid-state, and possess excellent thermal stability in air up to nearly 300 °C. This combination of physical properties, coupled with the ease of synthesis and the inexpensive, non-toxic nature of bismuth, make this class of inorganic-organic hybrid materials potentially promising for reversible smart window applications, camouflage coatings, temperature sensing, photocatalysis, color filters and displays.

Electrophilic organic selenium reagents - Protonated seleninic acids as precursors for unsymmetrical aromatic selenides

Stuhr-Hansen, Nicolai,S?lling, Theis Ivan,Henriksen, Lars

experimental part, p. 2633 - 2643 (2011/04/25)

Arylselenylations of methylbenzenes, methoxybenzenes and thiophene were smoothly achieved with selenenium ions generated by comproportionation of 1:1 mixtures of p-toluenesulfonic acid salts of seleninic acids and the corresponding diselenides. A series of p-toluenesulfonic salts of seleninic acids were prepared by hydrogen peroxide oxidation of the corresponding diselenides in the presence of p-toluenesulfonic acid. Novel 2-(organylseleno)thiophenes were obtained by heating the protonated seleninic acids with a 50-fold excess of thiophene in glacial acetic acid.

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