Never Underestimate The Influence Of Phenyl(pyridin-2-yl)methanone

COA of Formula: C12H9NO. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.

COA of Formula: C12H9NO. Batori, S; Csanyi, D; Takacs, D; Egyed, O; Riedl, Z; Hajos, G in [Batori, Sandor; Csanyi, Dorottya; Takacs, Daniella; Riedl, Zsuzsanna; Hajos, Gyorgy] Hungarian Acad Sci, Inst Organ Chem, Res Ctr Nat Sci, Magyar Tudosok Korutja 2, H-1117 Budapest, Hungary; [Egyed, Orsolya] Hungarian Acad Sci, Res Ctr Nat Sci, NMR Res Lab Instrumentat Ctr, Magyar Tudosok Korutja 2, H-1117 Budapest, Hungary; [Batori, Sandor] Rakoczi F Ut 268-A, H-1214 Budapest, Hungary published Synthetic procedure to pyrido[2,1-f][1,2,4]triazinium salt and related compounds in 2019.0, Cited 19.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

N-aminopyridyl ketone salts were reacted with formamide to yield heteroaromatic pyrido[2,1-f][1,2,4] triazinium salts. Upon storage of these products in the presence of water, formation of covalent hydrates have been observed. Reaction of the same starting compound with urethane yielded 3-chloropyrido[2,1-f][1,2,4]triazinium salt which readily reacted with secondary amines to afford 3-amino derivatives. An analogous ring closure reaction of 2-formylaminomethyl- and formaminobenzylpyridine allowed the synthesis of the partially reduced 3,4-dihydropyrido[2,1-f][1,2,4]triazinium compounds. The cyclization procedure was also applied for the synthesis of the related pyrimido[2,1-f][1,2,4]triazinium salt. (C) 2018 Elsevier Ltd. All rights reserved.

COA of Formula: C12H9NO. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem