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Cathodic behavior of 4,5‐dimethoxy‐2‐nitroamphetamine
Author(s) -
Squella J. A.,
Pezzani M.,
Cassels Bruce K.,
AillonTorres Milton,
Rezende Marcos C.,
NuñezVergara L. J.
Publication year - 1992
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.1140040508
Subject(s) - hydroxylamine , polarography , cathodic protection , nitro , chemistry , derivative (finance) , cyclic voltammetry , amphetamine , voltammetry , organic chemistry , electrochemistry , inorganic chemistry , electrode , psychology , alkyl , neuroscience , financial economics , dopamine , economics
The amphetamine derivative 4,5‐dimethoxy‐2‐nitrophenyl‐2‐aminopropane, a positional isomer of the potent hallucinogen DON, was studied by cyclic voltammetry and polarography. The nitro compound was reduced to the corresponding hydroxylamine under the experimental conditions used.