Attaryan, O. S. et al. published their research in Russian Journal of Organic Chemistry in 2006 | CAS: 15953-73-8

4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. 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 15953-73-8

Structure of the products of acrolein reactions with pyrazoles was written by Attaryan, O. S.;Antanosyan, S. K.;Kinoyan, F. S.;Tamazyan, R. A.;Panosyan, G. A.;Matsoyan, S. G.. And the article was included in Russian Journal of Organic Chemistry in 2006.Application of 15953-73-8 This article mentions the following:

Pyrazoles reacted with acrolein to give p1-pyrazolepropanals in fairly high yields. 3,5-Dimethyl-1-pyrazolepropanal dimerized on standing to the oxygen-linked dimer which on treatment with H2NOH gave 3,5-dimethyl-1-pyrazolepropanal oxime. In the experiment, the researchers used many compounds, for example, 4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8Application of 15953-73-8).

4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. 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 15953-73-8

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