Please use this identifier to cite or link to this item:
Title: Reationary ability of 3,5-Dibromo-N-Phenylanthranilic acids Derivatives
Authors: Alferova, D. A.
Алферова, Д. О.
Алферова, Д. А.
Svechnikova, E. N.
Свєчнікова, О. М.
Свечникова, Е. Н.
Suleiman, M. M.
Сулейман, М. М.
Сулейман, М. М.
Gritsenko, I. S.
Гриценко, І. С.
Гриценко, И. С.
Kazakov, G. P.
Казаков, Г. П.
Popova, N. V.
Попова, Н. В.
Kiz, O. V.
Кізь, О. В.
Кизь, О. В.
Yaremenko, V. D.
Яременко, В. Д.
Keywords: Anthranilic acid;reationary ability;acid-base properties;titration;Hammett’s equation
Issue Date: 2018
Publisher: Research J. Pharm. and Tech.
Bibliographic description (Ukraine): Reationary ability of 3,5-Dibromo-N-Phenylanthranilic acids Derivatives / D. A. Alferova, E. N. Svechnikova, M. M. Suleiman, I. S. Gritsenko, G. P. Kazakov, N. V. Popova, O. V. Kiz, V. D. Yaremenko // Research J. Pharm. and Tech. – 2018. – № 11 (9). – P. 1-3.
Abstract: The study of the acid-base properties of substituted N-phenylanthranilic acid is the important since, because it will allow the design of medicinal substances of this series with already known predictive properties. Therefore we have been studiedthe reactivity of 3,5-dibromo-N-phenylanthranilic acids has been studied. Reactivity of this isostructural group is studied in reversible conditions. The acid-base properties of 11 substituted of 3,5-dibromo-N-phenylanthranilic acids have been studied in a mixed solvent of dioxane-water (60 vol. % dioxane) at 25 С. It has been established that substitutes and their position in non-anthranilic fragment of a molecule influence on the avidity of these acids.
Appears in Collections:Наукові публікації кафедри медичної хiмiї

Files in This Item:
File Description SizeFormat 
Article_RJPT-6539-23-06-2018.pdf149,06 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.