Cargando…
tert-Butyl N-(thiophen-2-yl)carbamate
In the title compound, C(9)H(13)NO(2)S, the dihedral angle between the thiophene ring and the carbamate group is 15.79 (14)°. In the crystal structure, intramolecular C—H⋯O interactions in tandem with the tert-butyl groups render the packing of adjacent molecules in the [001] direction nearly per...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884429/ https://www.ncbi.nlm.nih.gov/pubmed/24427049 http://dx.doi.org/10.1107/S160053681302196X |
_version_ | 1782298588787769344 |
---|---|
author | Hsu, Gene C. Singer, Laci M. Cordes, David B. Findlater, Michael |
author_facet | Hsu, Gene C. Singer, Laci M. Cordes, David B. Findlater, Michael |
author_sort | Hsu, Gene C. |
collection | PubMed |
description | In the title compound, C(9)H(13)NO(2)S, the dihedral angle between the thiophene ring and the carbamate group is 15.79 (14)°. In the crystal structure, intramolecular C—H⋯O interactions in tandem with the tert-butyl groups render the packing of adjacent molecules in the [001] direction nearly perpendicular [the angle between adjacent thiophene rings is 74.83 (7)°]. An intermolecular N—H⋯O hydrogen bond gives rise to a chain extending along [001]. The crystal studied was found to be a racemic twin. |
format | Online Article Text |
id | pubmed-3884429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-38844292014-01-14 tert-Butyl N-(thiophen-2-yl)carbamate Hsu, Gene C. Singer, Laci M. Cordes, David B. Findlater, Michael Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(9)H(13)NO(2)S, the dihedral angle between the thiophene ring and the carbamate group is 15.79 (14)°. In the crystal structure, intramolecular C—H⋯O interactions in tandem with the tert-butyl groups render the packing of adjacent molecules in the [001] direction nearly perpendicular [the angle between adjacent thiophene rings is 74.83 (7)°]. An intermolecular N—H⋯O hydrogen bond gives rise to a chain extending along [001]. The crystal studied was found to be a racemic twin. International Union of Crystallography 2013-08-14 /pmc/articles/PMC3884429/ /pubmed/24427049 http://dx.doi.org/10.1107/S160053681302196X Text en © Hsu et al. 2013 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 Hsu, Gene C. Singer, Laci M. Cordes, David B. Findlater, Michael tert-Butyl N-(thiophen-2-yl)carbamate |
title |
tert-Butyl N-(thiophen-2-yl)carbamate |
title_full |
tert-Butyl N-(thiophen-2-yl)carbamate |
title_fullStr |
tert-Butyl N-(thiophen-2-yl)carbamate |
title_full_unstemmed |
tert-Butyl N-(thiophen-2-yl)carbamate |
title_short |
tert-Butyl N-(thiophen-2-yl)carbamate |
title_sort | tert-butyl n-(thiophen-2-yl)carbamate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884429/ https://www.ncbi.nlm.nih.gov/pubmed/24427049 http://dx.doi.org/10.1107/S160053681302196X |
work_keys_str_mv | AT hsugenec tertbutylnthiophen2ylcarbamate AT singerlacim tertbutylnthiophen2ylcarbamate AT cordesdavidb tertbutylnthiophen2ylcarbamate AT findlatermichael tertbutylnthiophen2ylcarbamate |