Modeling chemical reactions helps engineers virtually understand the chemistry, optimal size and design of the system, and how it interacts with other physics that may come into play. In an article, author is Franek, W, once mentioned the application of 21436-98-6, Name is 2,6-Dimethylaniline hydrochloride, molecular formula is C8H12ClN, molecular weight is 157.64, MDL number is MFCD00060213, category is thiomorpholine. Now introduce a scientific discovery about this category, Application of 21436-98-6.
In a new, feasible procedure five symmetrical para-substituted diaroylmethanes ((4-X-C6H4-CO)(2)-CH2; X = F, Cl, Br, CH3, and CH3O) are prepared, in most cases in very good yields. For purification and activation, they are converted into the copper(II) complexes of their enolates. Subsequently, three reaction steps with disulfur dichloride (S2Cl2), chlorine, and ethanethioic acid yield new CH-acidic dithio-bis-(diaroylmethanes), alpha-chlorosulfenic acid chlorides, and acetyl diaroylchloromethyl disulfides. The latter compounds are of interest for the liberation of highly reactive dithiirane/thiosulfine species. With thiomorpholine, alpha-chlorosulfenic acid chlorides give alpha-chlorosulfenic acid amides.
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Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem