More research is needed about 83846-85-9

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 83846-85-9. Category: thiomorpholine.

Chemistry, like all the natural sciences, Category: thiomorpholine, begins with the direct observation of nature¡ª in this case, of matter.83846-85-9, Name is Phenyl(4-(p-tolylthio)phenyl)methanone, SMILES is O=C(C1=CC=CC=C1)C2=CC=C(SC3=CC=C(C)C=C3)C=C2, belongs to thiomorpholine compound. In a document, author is Marcaccini, S, introduce the new discover.

Synthesis of thiomorpholines by an intramolecular Ugi reaction

The Ugi four-component condensation between 5-oxo-3-thiacarboxylic acids, benzylamines and cyclohexyl isocyanide gave 5-oxothiomorpholine-3-carboxamides. The configuration of bicyclic thiomorpholine derivatives was established by NOESY experiments. (C) 2002 Elsevier Science Ltd. All rights reserved.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 83846-85-9. Category: thiomorpholine.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem