Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 459-56-3, Name is (4-Fluorophenyl)methanol, SMILES is OCC1=CC=C(F)C=C1, in an article , author is Regiec, Andrzej, once mentioned of 459-56-3, Name: (4-Fluorophenyl)methanol.
New Amides of 5-(4-Chlorobenzoyl)aminoorotic Acid: Their Synthesis and Biological Activity
The synthesis and in-vitro biological evaluation of the amide series 4 of 5-(4-chlorobenzoyl)aminoorotic acid 2 are presented. The biological properties of a few 5-(4-chlorobenzoyl)amino-2,6-dihydroxy-N-substituted-4-pyrimidinecarboxamide derivatives 4 tested here were compared with derivatives 4 tested here were compared with those of the isosteric isothiazole derivative MR-2/94 (5-(4-chlorobenzoyl)amino-N-(4-chorophenyl)-3-methyl-4-isothiazolecarboxamide), which possesses a strong immunosuppressive and anti-inflammatory activity [1, 2], It must be suggested that replacement of the isothiazole by a pyrimidine core ring system resulted in considerable lowering of the anti-inflammatory and immunotropic actions of the obtained amides. Physicochemical properties of 2-(4-chlorophenyl)-6, 8-dihydroxy-4H-pyrimido[5,4-d]-1,3-oxazin-4-on 3 are also briefly described.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 459-56-3, you can contact me at any time and look forward to more communication. Name: (4-Fluorophenyl)methanol.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com