Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate

The title compound, C(8)H(11)NO(2)S, crystallizes with two mol­ecules, A and B, in the asymmetric unit. Each molecule features an intramolecular N—H⋯O hydrogen bond and the same H atom is also involved in an intermolecular N—H⋯S bond to generate A + B dimers. Further N—H⋯O hydrogen bonds link the di...

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Autores principales: Khanum, Ghazala, Fatima, Aysha, Sharma, Pooja, Srivastava, S. K., Butcher, Ray J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462330/
https://www.ncbi.nlm.nih.gov/pubmed/36339105
http://dx.doi.org/10.1107/S2414314621003515
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author Khanum, Ghazala
Fatima, Aysha
Sharma, Pooja
Srivastava, S. K.
Butcher, Ray J.
author_facet Khanum, Ghazala
Fatima, Aysha
Sharma, Pooja
Srivastava, S. K.
Butcher, Ray J.
author_sort Khanum, Ghazala
collection PubMed
description The title compound, C(8)H(11)NO(2)S, crystallizes with two mol­ecules, A and B, in the asymmetric unit. Each molecule features an intramolecular N—H⋯O hydrogen bond and the same H atom is also involved in an intermolecular N—H⋯S bond to generate A + B dimers. Further N—H⋯O hydrogen bonds link the dimers into a [010] chain. [Image: see text]
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spelling pubmed-94623302022-11-04 Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate Khanum, Ghazala Fatima, Aysha Sharma, Pooja Srivastava, S. K. Butcher, Ray J. IUCrdata Data Reports The title compound, C(8)H(11)NO(2)S, crystallizes with two mol­ecules, A and B, in the asymmetric unit. Each molecule features an intramolecular N—H⋯O hydrogen bond and the same H atom is also involved in an intermolecular N—H⋯S bond to generate A + B dimers. Further N—H⋯O hydrogen bonds link the dimers into a [010] chain. [Image: see text] International Union of Crystallography 2021-04-09 /pmc/articles/PMC9462330/ /pubmed/36339105 http://dx.doi.org/10.1107/S2414314621003515 Text en © Khanum et al. 2021 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Khanum, Ghazala
Fatima, Aysha
Sharma, Pooja
Srivastava, S. K.
Butcher, Ray J.
Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title_full Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title_fullStr Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title_full_unstemmed Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title_short Ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
title_sort ethyl 2-amino-4-methyl­thio­phene-3-carboxyl­ate
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462330/
https://www.ncbi.nlm.nih.gov/pubmed/36339105
http://dx.doi.org/10.1107/S2414314621003515
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AT fatimaaysha ethyl2amino4methylthiophene3carboxylate
AT sharmapooja ethyl2amino4methylthiophene3carboxylate
AT srivastavask ethyl2amino4methylthiophene3carboxylate
AT butcherrayj ethyl2amino4methylthiophene3carboxylate

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