N-Cyclo­hexyl-N-propyl­benzene­sulfonamide

The title compound, C(15)H(23)NO(2)S, synthesized by N-methyl­ation of cyclo­hexyl­amine sulfonamide with propyl iodide, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo­hexyl ring exists in the chair form and the dihedral angle between the ri...

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Detalles Bibliográficos
Autores principales: Haider, Zeeshan, Khan, Islam Ullah, Zia-ur-Rehman, Muhammad, Arshad, Muhammad Nadeem
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971915/
https://www.ncbi.nlm.nih.gov/pubmed/21578881
http://dx.doi.org/10.1107/S1600536809046650
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author Haider, Zeeshan
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
author_facet Haider, Zeeshan
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
author_sort Haider, Zeeshan
collection PubMed
description The title compound, C(15)H(23)NO(2)S, synthesized by N-methyl­ation of cyclo­hexyl­amine sulfonamide with propyl iodide, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo­hexyl ring exists in the chair form and the dihedral angle between the ring plane of the benzene ring and that of the cyclo­hexyl ring is 50.13 (9)°.
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spelling pubmed-29719152010-12-30 N-Cyclo­hexyl-N-propyl­benzene­sulfonamide Haider, Zeeshan Khan, Islam Ullah Zia-ur-Rehman, Muhammad Arshad, Muhammad Nadeem Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(23)NO(2)S, synthesized by N-methyl­ation of cyclo­hexyl­amine sulfonamide with propyl iodide, is of inter­est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo­hexyl ring exists in the chair form and the dihedral angle between the ring plane of the benzene ring and that of the cyclo­hexyl ring is 50.13 (9)°. International Union of Crystallography 2009-11-21 /pmc/articles/PMC2971915/ /pubmed/21578881 http://dx.doi.org/10.1107/S1600536809046650 Text en © Haider 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
Haider, Zeeshan
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Arshad, Muhammad Nadeem
N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title_full N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title_fullStr N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title_full_unstemmed N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title_short N-Cyclo­hexyl-N-propyl­benzene­sulfonamide
title_sort n-cyclo­hexyl-n-propyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971915/
https://www.ncbi.nlm.nih.gov/pubmed/21578881
http://dx.doi.org/10.1107/S1600536809046650
work_keys_str_mv AT haiderzeeshan ncyclohexylnpropylbenzenesulfonamide
AT khanislamullah ncyclohexylnpropylbenzenesulfonamide
AT ziaurrehmanmuhammad ncyclohexylnpropylbenzenesulfonamide
AT arshadmuhammadnadeem ncyclohexylnpropylbenzenesulfonamide

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