N-(Adamantan-1-yl)-2-chloro­acetamide

In the title compound, C(12)H(18)ClNO, which was synthesized as part of a study into potential anti­tuberculosis agents, the adamantine skeleton displays shorter than normal C—C bond lengths ranging between 1.5293 (18) and 1.5366 (15) Å. The structure also displays inter­molecular N—H⋯O hydrogen bon...

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Detalles Bibliográficos
Autores principales: Onajole, Oluseye K., Govender, Thavendran, Kruger, Hendrik G., Maguire, Glenn E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120360/
https://www.ncbi.nlm.nih.gov/pubmed/21754821
http://dx.doi.org/10.1107/S1600536811018046
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author Onajole, Oluseye K.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_facet Onajole, Oluseye K.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_sort Onajole, Oluseye K.
collection PubMed
description In the title compound, C(12)H(18)ClNO, which was synthesized as part of a study into potential anti­tuberculosis agents, the adamantine skeleton displays shorter than normal C—C bond lengths ranging between 1.5293 (18) and 1.5366 (15) Å. The structure also displays inter­molecular N—H⋯O hydrogen bonding, which forms an infinite chain in the a-axis direction.
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spelling pubmed-31203602011-07-13 N-(Adamantan-1-yl)-2-chloro­acetamide Onajole, Oluseye K. Govender, Thavendran Kruger, Hendrik G. Maguire, Glenn E. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(18)ClNO, which was synthesized as part of a study into potential anti­tuberculosis agents, the adamantine skeleton displays shorter than normal C—C bond lengths ranging between 1.5293 (18) and 1.5366 (15) Å. The structure also displays inter­molecular N—H⋯O hydrogen bonding, which forms an infinite chain in the a-axis direction. International Union of Crystallography 2011-05-20 /pmc/articles/PMC3120360/ /pubmed/21754821 http://dx.doi.org/10.1107/S1600536811018046 Text en © Onajole et al. 2011 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
Onajole, Oluseye K.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
N-(Adamantan-1-yl)-2-chloro­acetamide
title N-(Adamantan-1-yl)-2-chloro­acetamide
title_full N-(Adamantan-1-yl)-2-chloro­acetamide
title_fullStr N-(Adamantan-1-yl)-2-chloro­acetamide
title_full_unstemmed N-(Adamantan-1-yl)-2-chloro­acetamide
title_short N-(Adamantan-1-yl)-2-chloro­acetamide
title_sort n-(adamantan-1-yl)-2-chloro­acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120360/
https://www.ncbi.nlm.nih.gov/pubmed/21754821
http://dx.doi.org/10.1107/S1600536811018046
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AT krugerhendrikg nadamantan1yl2chloroacetamide
AT maguireglennem nadamantan1yl2chloroacetamide

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