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14132-13-9

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14132-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14132-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14132-13:
(7*1)+(6*4)+(5*1)+(4*3)+(3*2)+(2*1)+(1*3)=59
59 % 10 = 9
So 14132-13-9 is a valid CAS Registry Number.

14132-13-9Downstream Products

14132-13-9Relevant academic research and scientific papers

Reaction of singlet oxygen with thioanisole in ionic liquids: A solvent induced mechanistic dichotomy

Baciocchi, Enrico,Chiappe, Cinzia,Del Giacco, Tiziana,Fasciani, Chiara,Lanzalunga, Osvaldo,Lapi, Andrea,Melai, Bernardo

, p. 1413 - 1416 (2009)

A study of the reaction of thioanisole with singlet oxygen in pyrrolidinium-and imidazolium-based ionic liquids has been carried out. In these solvents, thioanisole shows a strongly enhanced reactivity with respect to molecular aprotic solvents, probably

A novel synthesis of aryl methyl sulfones and β-hydroxysulfones from sodium sulfinates and di-tert-butyl peroxide in H2O medium

Lai, Junyi,Yuan, Gaoqing

, p. 524 - 527 (2018/01/10)

A novel and convenient synthetic route for aryl methyl sulfones and β-hydroxysulfones was developed via the radical reaction between sodium sulfinates and di-tert-butyl peroxide (DTBP). Without any catalysts and additives, the synthetic process could be smoothly carried out to afford the target products in good to excellent yields in H2O medium, demonstrating its promising application. In the present system, H2O could act not only as a green solvent but also as a reactant.

Evidence for the involvement of a sulfurane intermediate in the oxidation of simple sulfides by methyl(trifluoromethyl)dioxirane

Asensio, Gregorio,Mello, Rossella,Gonzalez-Nunez, Maria Elena

, p. 2299 - 2302 (2007/10/03)

Methyl(trifluoromethyl)dioxirane reacts with sulfides to give preferentially sulfones, even in the presence of competing sulfoxides. The sulfoxide yield increases at the expense of the sulfone when 2,2,2-trifluoroethanol is used as co-solvent. The reactio

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