tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate

The title compound, C(11)H(21)Cl(3)N(2)O(4)S, was produced as part of a development programme of a new synthetic route to chloro­ethyl­nitro­sosulfamides (CENS) with three chloro­ethyl moieties. These compounds possess structural features that confer potential biological activity and act as alkyl­at...

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Detalles Bibliográficos
Autores principales: Seridi, Achour, Akkari, Hocine, Winum, Jean-Yves, Bénard-Rocherullé, Patricia, Abdaoui, Mohamed
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970185/
https://www.ncbi.nlm.nih.gov/pubmed/21577986
http://dx.doi.org/10.1107/S1600536809038185
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author Seridi, Achour
Akkari, Hocine
Winum, Jean-Yves
Bénard-Rocherullé, Patricia
Abdaoui, Mohamed
author_facet Seridi, Achour
Akkari, Hocine
Winum, Jean-Yves
Bénard-Rocherullé, Patricia
Abdaoui, Mohamed
author_sort Seridi, Achour
collection PubMed
description The title compound, C(11)H(21)Cl(3)N(2)O(4)S, was produced as part of a development programme of a new synthetic route to chloro­ethyl­nitro­sosulfamides (CENS) with three chloro­ethyl moieties. These compounds possess structural features that confer potential biological activity and act as alkyl­ating agents. The packing is governed by four weak C—H⋯O inter­actions, forming an infinite three-dimensional network.
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spelling pubmed-29701852010-12-30 tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate Seridi, Achour Akkari, Hocine Winum, Jean-Yves Bénard-Rocherullé, Patricia Abdaoui, Mohamed Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(21)Cl(3)N(2)O(4)S, was produced as part of a development programme of a new synthetic route to chloro­ethyl­nitro­sosulfamides (CENS) with three chloro­ethyl moieties. These compounds possess structural features that confer potential biological activity and act as alkyl­ating agents. The packing is governed by four weak C—H⋯O inter­actions, forming an infinite three-dimensional network. International Union of Crystallography 2009-09-26 /pmc/articles/PMC2970185/ /pubmed/21577986 http://dx.doi.org/10.1107/S1600536809038185 Text en © Seridi et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Seridi, Achour
Akkari, Hocine
Winum, Jean-Yves
Bénard-Rocherullé, Patricia
Abdaoui, Mohamed
tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title_full tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title_fullStr tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title_full_unstemmed tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title_short tert-Butyl N-[N,N-bis­(2-chloro­ethyl)sulfamo­yl]-N-(2-chloro­ethyl)carbamate
title_sort tert-butyl n-[n,n-bis­(2-chloro­ethyl)sulfamo­yl]-n-(2-chloro­ethyl)carbamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970185/
https://www.ncbi.nlm.nih.gov/pubmed/21577986
http://dx.doi.org/10.1107/S1600536809038185
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AT abdaouimohamed tertbutylnnnbis2chloroethylsulfamoyln2chloroethylcarbamate

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