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This compound(3-(Chloromethyl)-1-methyl-1H-pyrazole)Product Details of 84547-64-8 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called 1,3- And 1,5-dimethylpyrazole-based syntheses. VI. Stilbene and 1,4-distyrylbenzene analogs containing 3-, 4-, and 5-pyrazolyl radicals, published in 1982-11-30, which mentions a compound: 84547-64-8, Name is 3-(Chloromethyl)-1-methyl-1H-pyrazole, Molecular C5H7ClN2, Product Details of 84547-64-8.

Condensation of 4-O2NC6H4CH2CO2H with pyrazolecarboxaldehydes, followed by reduction with SnCl2, gave I (R, R1 = H, H; Me, H; H, Me). Appropriate Wittig reactions gave II (R = 1-methyl-3-pyrazolyl, 4,5-dichloro-1-methyl-3-pyrazolyl, 1-methyl-5-pyrazolyl, 4-chloro-1-methyl-5-pyrazolyl), which showed intensive blue fluorescence in PhMe solution

This compound(3-(Chloromethyl)-1-methyl-1H-pyrazole)Product Details of 84547-64-8 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

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