You Should Know Something about 4-(1,2,4-Triazol-1-yl)aniline

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 4-(1,2,4-Triazol-1-yl)aniline, in my other articles.

Research speed reading in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 6523-49-5, name is 4-(1,2,4-Triazol-1-yl)aniline belongs to triazoles compound, it is a common compound, a new synthetic route is introduced below. 6523-49-5

The formamidine from Step 1 (100 mg) and 4-triazolylaniline (73 mg) in AcOH(3 ml) were heated at 125 for 3 h. The cooled reaction mixture was concentrated and purified by column chromatography on silica gel with DCM:MeOH (2.5 %) as eluant. This gave the product (54 mg).1H NMR delta 10.14 (IH, s), 9.28 (IH, s), 8.87 (IH, s), 8.62 (IH, s), 8.25 (2H, m),8.06 (2H, m), 7.9 (4H, m), 7.16 (IH, m), 6.73 (IH, m); LC-MS rt 2.25 m/z 353 ES-.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 4-(1,2,4-Triazol-1-yl)aniline, in my other articles.

Reference:
Patent; ARROW THERAPEUTICS LIMITED; WO2007/80401; (2007); A1;,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics