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"Benzene, [[2-(methylseleno)ethenyl]seleno]-, (Z)-" is a complex organic compound characterized by a benzene ring with a unique selenium-containing side chain. The molecule features a (Z)-configuration, indicating the geometric arrangement of the double bonds. The side chain consists of a vinyl group (ethenyl) with a methyl group attached to the selenium atom, which is further connected to another selenium atom. Benzene, [[2-(methylseleno)ethenyl]seleno]-, (Z)- is of interest in the field of organoselenium chemistry due to its potential applications in materials science and as a precursor in the synthesis of other organoselenium compounds. It is important to note that the handling and use of such compounds should be done with caution, as they may have specific safety and environmental considerations.

7392-16-7

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7392-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7392-16-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 7392-16:
(6*7)+(5*3)+(4*9)+(3*2)+(2*1)+(1*6)=107
107 % 10 = 7
So 7392-16-7 is a valid CAS Registry Number.

7392-16-7Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF DIVINYL DISELENIDES FROM VINYL ACETYL SELENIDES

Testaferri, Lorenzo,Tiecco, Marcello,Chianelli, Donatella,Tingoli, Marco

, p. 4577 - 4584 (2007/10/02)

Vinyl halides react with MeSeLi in DMF to afford vinyl methyl selenides which are demethylated by the excess of the MeSeLi; the vinyl selenide anions thus obtained react with acetyl chloride to give vinyl acetyl selenides.This three steps one pot synthesis occurs with complete retention of configuration.The vinyl acetyl selenides are cleanly fragmented by electron transfer to the vinyl selenide anions; addition of iodine to the resulting solutions produced the divinyl diselenides with retention of configuration.The transformation of vinyl acetyl selenides into divinyl diselenides can also be induced by catalytic amounts of a solution of sodium in HMPA or of sodium methanethiolate.

NEW SYNTHESIS OF VINYL SELENIDES NUCLEOPHILIC SUBSTITUTIONS OF UNACTIVATED VINYL HALIDES BY SELENIDE ANIONS

Tiecco, M.,Testaferri, L.,Tingoli, M.,Chianelli, D.,Montanucci, M.

, p. 4975 - 4978 (2007/10/02)

Alkyl and aryl selenide anions react with unactivated vinyl halides, in dipolar aprotic solvents, to give alkyl or aryl vinyl selenides in good yields.These reactions are stereospecific and occur with retention of configuration.

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