Flexible application of in synthetic route 84547-64-8

In some applications, this compound(84547-64-8)Reference of 3-(Chloromethyl)-1-methyl-1H-pyrazole is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 84547-64-8, is researched, SMILESS is CN1N=C(CCl)C=C1, Molecular C5H7ClN2Journal, Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii) called New synthesis and properties of 3-alkyl-, 3-chloroalkyl-, 3-perfluoroalkyl-, and 3-aryl-1-methyl-5-halopyrazoles from chloro(bromo)vinyl ketones and N,N-dimethylhydrazine, Author is Levkovskaya, G. G.; Bozhenkov, G. V.; Larina, L. I.; Mirskova, A. N., the main research direction is regioselective heterocyclization halovinyl ketone dimethylhydrazine; halopyrazole preparation; pyrazole halo preparation.Reference of 3-(Chloromethyl)-1-methyl-1H-pyrazole.

A new regioselective heterocyclization was revealed in the reaction of 2-chloro- and 2,2-dichloro(bromo)vinyl ketones with N,N-dimethylhydrazine to afford 3-substituted 1-methyl-5-halopyrazoles. The reaction is accompanied by elimination of Me halide and formation of up to 90% of N,N,N-trimethylhydrazinium halide as the second product.

In some applications, this compound(84547-64-8)Reference of 3-(Chloromethyl)-1-methyl-1H-pyrazole is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics