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(3-fluorophenyl)(trifluoromethyl)selane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15875-68-0

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15875-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15875-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15875-68:
(7*1)+(6*5)+(5*8)+(4*7)+(3*5)+(2*6)+(1*8)=140
140 % 10 = 0
So 15875-68-0 is a valid CAS Registry Number.

15875-68-0Downstream Products

15875-68-0Relevant academic research and scientific papers

Difluoro(aryl)(perfluoroalkyl)-λ4-sulfanes and Selanes: Missing Links of Trichloroisocyanuric Acid/Potassium Fluoride Chemistry

Brüning, Fabian,Pitts, Cody Ross,Kalim, Jorna,Bornemann, Dustin,Ghiazza, Clément,de Montmollin, Jean,Trapp, Nils,Billard, Thierry,Togni, Antonio

supporting information, p. 18937 - 18941 (2019/11/26)

The TCICA/KF approach to oxidative fluorination of heteroatoms has emerged as a surprisingly simple, safe, and versatile surrogate to classically challenging fluorination reactions. Although polyfluorination (or chlorofluorination) of diaryl disulfides, diaryl diselenides, diaryl ditellurides, aryl iodides, and aryl(perfluoroalkyl)tellanes has been described, the application of this TCICA/KF methodology to aryl(perfluoroalkyl)sulfanes and selanes remains an area of unexplored chemical space. Accordingly, to address the “missing links” in the developing series of chalcogen-based substrate reactivity, we report mild syntheses of metastable difluoro(aryl)(perfluoroalkyl)-λ4-sulfanes and selanes. As only limited examples of these species exist in the current literature (accessible only by using F2 or XeF2/HF), we have carried out detailed structural analyses, primarily using NMR and SC-XRD data. In addition, we investigate the effect of the perfluoroalkyl chain on the outcome of oxidative fluorination, and, finally, we provide preliminary evidence that difluoro(aryl)(trifluoro-methyl)-λ4-sulfanes may act as fluorinating reagents.

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