Literature DB >> 26694797

Oxidation of 2-aminophenol to 2-amino-3H-phenoxazin-3-one with monochloramine in aqueous environment: A new method for APO synthesis?

Odissa Abou Mehrez1, Florence Dossier-Berne2, Bernard Legube2.   

Abstract

Reaction of 2-aminophenol (2AP) with monochloramine in aqueous solution was investigated at pH 8.5 and 25 °C, with an excess of monochloramine. 2-Amino-3H-phenoxazin-3-one (APO) was the major product formed in about 70% yield. Despite low formation yields, adsorbable organic halides (AOX) were also formed over reaction time.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  2-Amino-3H-phenoxazin-3-one; 2-Aminophenol; Adsorbable organic halides; Monochloramine

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Substances：

Year:  2015        PMID： 26694797     DOI： 10.1016/j.chemosphere.2015.11.073

Source DB:  PubMed          Journal:  Chemosphere        ISSN： 0045-6535            Impact factor:   7.086


  3 in total

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Journal:  World J Microbiol Biotechnol       Date:  2019-10-31       Impact factor: 3.312

2.  Synthesis of highly crystalline LaFeO3 nanospheres for phenoxazinone synthase mimicking activity.

Authors:  Mohamed Khairy; Abdelrahman H Mahmoud; Kamal M S Khalil
Journal:  RSC Adv       Date:  2021-05-17       Impact factor: 4.036

3.  A taxonomically representative strain collection to explore xenobiotic and secondary metabolism in bacteria.

Authors:  Evanthia Kontomina; Vasiliki Garefalaki; Konstantina C Fylaktakidou; Dorothea Evmorfidou; Athina Eleftheraki; Marina Avramidou; Karen Udoh; Maria Panopoulou; Tamás Felföldi; Károly Márialigeti; Giannoulis Fakis; Sotiria Boukouvala
Journal:  PLoS One       Date:  2022-07-14       Impact factor: 3.752
  3 in total

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