Category: 58498-61-6

De Kowalewski, D. G.’s team published research in Journal of Molecular Structure in 1989 | CAS: 58498-61-6

5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.HPLC of Formula: 58498-61-6

HPLC of Formula: 58498-61-6On October 31, 1989 ,《Carbon-13 and proton NMR spectra of 2-pyridone derivatives》 appeared in Journal of Molecular Structure. The author of the article were De Kowalewski, D. G.; Contreras, R. H.; De los Santos, C.. The article conveys some information:

The 13C- and 1H-NMR of substituted pyridines (e.g. I) were studied to determine through additivity properties of 13C shielding constants and of the 13C-1H spin-spin coupling constants, the structure of the ring and of the lateral chains. In the part of experimental materials, we found many familiar compounds, such as 5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6HPLC of Formula: 58498-61-6)

5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.HPLC of Formula: 58498-61-6

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Sepiol, Jadwiga’s team published research in Universitatis Iagellonicae Acta Chimica in 1991 | CAS: 58498-61-6

5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Recommanded Product: 5-Chloro-3-methylpyridin-2-ol

《Syntheses with aromatic nitramines. Part VIII. Rearrangements of isomeric nitraminopyridines with aroyl chlorides》 was published in Universitatis Iagellonicae Acta Chimica in 1991. These research results belong to Sepiol, Jadwiga; Tomasik, Piotr. Recommanded Product: 5-Chloro-3-methylpyridin-2-ol The article mentions the following:

2-Nitraminopyridine reacts with BzCl to give 5-chloro-1H-pyridin-2-one. 4-Nitraminopyridine with the same reagent produces both 3-chloro-1H-pyridin-4-one and unsubstituted 1H-pyridin-4-one, and 3-nitraminopyridine gives solely 3-hydroxypyridine. Any substituent in the 5-position of 2-nitraminopyridine or an electron-withdrawing substituent in the 3-position of that nitramine prohibit chlorination in the β-position. The reaction is accelerated by electron-donating substituents in the acyl moiety and (4-MeOC6H4COCl) and slowed down by electron-withdrawing substituents, e.g. 4-O2NC6H4COCl. In the experiment, the researchers used 5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6Recommanded Product: 5-Chloro-3-methylpyridin-2-ol)

5-Chloro-3-methylpyridin-2-ol(cas: 58498-61-6) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Recommanded Product: 5-Chloro-3-methylpyridin-2-ol

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem