Abstract
1. Dinitroformaldehyde alkoxycarbonylhydrazones and pyridinium nitronate betaines were obtained for the first time. 2. The dinitroformaldehyde alkoxycarbonylhydrazones readily replace the nitro group by a halogen atom when treated with dry hydrogen chloride in ether or with potassium chloride in DMFA. 3. The ionization constants of the dinitro and chloronitroformaldehyde alkoxycarbonylhydrazones in water were determined.
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