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N-Ethyl substituted 2-nitrophenylguanidines. 1. Synthesis and properties

P. Pazdera and M. Potáček

Department of Organic Chemistry, Faculty of Natural Sciences, J. E. Purkyně University, CS-611 37 Brno

 

Abstract: New TV-mono-, di-, and triethyl substituted 2-nitrophenylguanidines with the ethyl group situated at nitrogen atom which does not adjoin 2-nitro-phenyl group were prepared. Dissociation constants of the synthesized compounds were determined by spectrophotometry. The structure of the most stable tautomer under conditions of measurement was proved by IR, 1H, and 13C NMR spectroscopy.

Full paper in Portable Document Format: 431a97.pdf

 

Chemical Papers 43 (1) 97–106 (1989)

Monday, July 22, 2019

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