Literature DB >> 16289822

Kinetic investigation on aqueous decomposition of 2-chloroethylnitrososulfamide.

Achour Seridi1, Mekki Kadri, Mohamed Abdaoui, Jean-Yves Winum, Jean-Louis Montero.   

Abstract

The kinetics decomposition of 2-chloroethylnitrososulfamides (CENS) was studied in aqueous buffered solutions with pH ranging from 0 to 14. The study was monitored by RP-LC-MS and conventional UV spectrophotometry. The reaction proceeded via a pseudo-first-order kinetic with significant correlation coefficient. The major decomposition products from CENS after incubation in phosphate buffer were isolated and identified by NMR and mass spectrometry. The results indicate that the mechanism pathway involves a denitrosation of the CENS and competitive hydrolysis with nucleophilic attack on the sulfur atom and formation of sulfamate compounds.

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Year:  2005        PMID: 16289822     DOI: 10.1016/j.bmcl.2005.10.080

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  tert-Butyl N-[N,N-bis-(2-chloro-ethyl)sulfamo-yl]-N-(2-chloro-ethyl)carbamate.

Authors:  Achour Seridi; Hocine Akkari; Jean-Yves Winum; Patricia Bénard-Rocherullé; Mohamed Abdaoui
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-09-26
  1 in total

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