The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Application In Synthesis of 4-(Trifluoromethyl)aniline, 455-14-1, Name is 4-(Trifluoromethyl)aniline, SMILES is C1=C(C(F)(F)F)C=CC(=C1)N, in an article , author is Haroune, N, once mentioned of 455-14-1.
H-1 NMR: a tool to study the fate of pollutants in the environment
In situ H-1 NMR, directly performed on biological fluids is a very powerful tool to study the fate of pollutants in the environment. The biodegradation of 2-aminobenzothiazole by Rhodococcus rhodochrous was monitored by reverse phase HPLC and by in situ H-1 NMR, methods performed directly on culture media without purification. The xenobiotic was biotransformed into a hydroxylated derivative. The chemical structure of this metabolite was determined by a long-range H-1-N-15 heteronuclear shift correlation without any previous N-15 enrichment of the compound. This approach allowed the assignment of the metabolite structure to 2-amino-6-hydroxybenzothiazole. (C) 2001 Academie des sciences/Editions scientifiques et medicates Elsevier SAS.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 455-14-1, you can contact me at any time and look forward to more communication. Application In Synthesis of 4-(Trifluoromethyl)aniline.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem