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1-(3-amino-4-((4-methoxyphenyl)thio)phenyl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19688-58-5

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19688-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19688-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,8 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19688-58:
(7*1)+(6*9)+(5*6)+(4*8)+(3*8)+(2*5)+(1*8)=165
165 % 10 = 5
So 19688-58-5 is a valid CAS Registry Number.

19688-58-5Downstream Products

19688-58-5Relevant academic research and scientific papers

PHOTOCATALYST-FREE, LIGHT-INDUCED CARBON-SULFUR CROSS-COUPLING METHODS

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Paragraph 0099; 0177; 0178, (2019/01/10)

In one aspect, the invention provides a method of promoting a carbon-sulfur bond forming reaction. In certain embodiments, the reaction comprises cross-coupling of a(n) (hetero)aryl halide with a thiol to form the carbon-sulfur bond, wherein the method is promoted by light irradiation in the absence of a photocatalyst. In other embodiments, the cross-coupling reaction can be promoted through visible light irradiation, including sunlight.

Visible-light-promoted C-S cross-coupling via intermolecular charge transfer

Liu, Bin,Lim, Chern-Hooi,Miyake, Garret M.

supporting information, p. 13616 - 13619 (2017/11/06)

Disclosed is a mild, scalable, visible-lightpromoted cross-coupling reaction between thiols and aryl halides for the construction of C-S bonds in the absence of both transition metal and photoredox catalysts. The scope of aryl halides and thiol partners includes over 60 examples and therefore provides an entry point into various aryl thioether building blocks of pharmaceutical interest. Furthermore, to demonstrate its utility, this C-S coupling protocol was applied in drug synthesis and latestage modifications of active pharmaceutical ingredients. UV-vis spectroscopy and time-dependent density functional theory calculations suggest that visible-lightpromoted intermolecular charge transfer within the thiolate-aryl halide electron donor-acceptor complex permits the reactivity in the absence of catalyst.

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