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Trans-1,2-bis(methylseleno)-1-phenylethylene is an organoselenium compound characterized by a phenylethylene backbone with two methylselenyl groups attached to the double bond in a trans configuration. This molecule is of interest in the field of organoselenium chemistry due to its potential applications in various areas, such as pharmaceuticals and materials science. The trans configuration implies that the two methylselenyl groups are positioned on opposite sides of the double bond, which can influence the molecule's reactivity and physical properties. Research on such compounds often focuses on their unique electronic and steric effects, as well as their potential to act as precursors to more complex selenium-containing molecules.

7392-17-8

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7392-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7392-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7392-17:
(6*7)+(5*3)+(4*9)+(3*2)+(2*1)+(1*7)=108
108 % 10 = 8
So 7392-17-8 is a valid CAS Registry Number.

7392-17-8Downstream Products

7392-17-8Relevant academic research and scientific papers

Thermal Reaction of Phenylacetylene with Dialkyl Diselenides

Shilkina, T. A.,Papernaya, L. K.,Deryagina, E. N.,Albanov, A. I.

, p. 77 - 79 (2007/10/03)

Heating of phenylacetylene with dialkyl diselenides results in addition of two alkaneselenyl groups to the phenylacetylene triple bond to give a mixture of E and Z adducts. When heated together with dialkyl disulfides, diakyl diselenides initiate addition

Organic Diselenides And Ditellurides: Disproportionations, Synthesis Of Stannyl Selenides, Reactions With Acetylenes

Potapov, Vladimir A.,Amosova, Svetlana V.,Beletskaya, Irina P.,Starkova, Anna A.,Hevesi, Laszlo

, p. 591 - 594 (2007/10/03)

The disproportionation reaction of organic diselenides 1 and ditellurides 2, the synthesis of stannyl selenides 4, and the addition reaction (palladium-catalyzed, thermal) of dialkyl diselenides to acetylenes are discussed.

77Se NMR. 2. The Basis for Application of JSe-Se and JSe-H in Structure Assignments of Mono-, Di-, and Triseleno-Substituted Alkenes

Johannsen, Ib,Henriksen, Lars,Eggert, Hanne

, p. 1657 - 1663 (2007/10/02)

Series of isomeric mono-, di-, and triseleno-substituted alkenes have been synthesized and subjected to 77Se NMR analysis.In di- and triseleno-substituted alkenes stereochemical assignments were obtained by measurements of 77Se-77Se coupling constants.Val

77Se NMR. Observation of3JSe-Se Couplings Allowing Cis/Trans Isomer Assignments in Substituted Tetraselenafulvalenes

Johannsen, Ib,Eggert, Hanne

, p. 1240 - 1243 (2007/10/02)

77Se chemical shifts and 1H-77Se and 77Se-77Se coupling constants are given for a series of substituted tetraselenafulvalenes (TSFs).For mixtures of cis and trans isomers resolved signals for each isomer were observed at 21 kG.The cis/trans assignments we

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