Hennig, Horst et al. published their research in Zeitschrift fuer Chemie in 1971 | CAS: 19959-77-4

2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazoles are commonly used scaffold molecules in drug discovery projects. The use of pyrazole derivatives is based on their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, sedative, muscle relaxant, neuroleptic, anticonvulsant, monoamine oxidase inhibitory, antidiabetic and antibacterial activities.Application of 19959-77-4

Coordination tendencies of acidic amino groups. VIII. Complexing behavior of 3-methyl-5-pyridyl-2-pyrazole was written by Hennig, Horst;Daute, Ingeborg. And the article was included in Zeitschrift fuer Chemie in 1971.Application of 19959-77-4 This article mentions the following:

3-Methyl-5-(2-pyridyl)pyrazole (HMPP) reacted with metal acetylacetonates to give the following complexes: [Cu(MPP)2], [Ni(MPP)2], [Co(MPP)3], [Zn(MPP)2], [Pd(MPP)2], (Cu(HMPP)Cl2] and [Co(HMPP)Cl2]. In the experiment, the researchers used many compounds, for example, 2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4Application of 19959-77-4).

2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazoles are commonly used scaffold molecules in drug discovery projects. The use of pyrazole derivatives is based on their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, sedative, muscle relaxant, neuroleptic, anticonvulsant, monoamine oxidase inhibitory, antidiabetic and antibacterial activities.Application of 19959-77-4

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics