Tretyakov, E. V. et al. published their research in Izvestiya Akademii Nauk, Seriya Khimicheskaya in 1996 | CAS: 54210-32-1

1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1) 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 can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.Safety of 1-Methyl-3-nitro-1H-pyrazole

Synthesis of vicinal aminoiodo- and (acetylamino)iodo-1-alkylpyrazoles was written by Tretyakov, E. V.;Vasilevsky, S. F.. And the article was included in Izvestiya Akademii Nauk, Seriya Khimicheskaya in 1996.Safety of 1-Methyl-3-nitro-1H-pyrazole This article mentions the following:

One-pot acylation-iodination of 3- and 5-amino-1-alkylpyrazoles gave 3- and 5-acetamido-4-iodo-1-alkylpyrazoles. Reduction of iodonitropyrazoles with SnCl2 in HCl gave 3- and 5-iodo- and 3,5-diiodo-4-amino-1-methylpyrazole. In the experiment, the researchers used many compounds, for example, 1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1Safety of 1-Methyl-3-nitro-1H-pyrazole).

1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1) 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 can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.Safety of 1-Methyl-3-nitro-1H-pyrazole

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