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Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate
In the title compound, C(16)H(17)NO(3)S, a thiophene derivative with amino phenyl, acetyl, methyl and ethyl carboxyl susbtituents attached to a central thiophene ring, the phenyl and thiophene rings form a dihedral angle of 36.92 (9) Å. The molecular conformation is stabilized by an intramolecu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772481/ https://www.ncbi.nlm.nih.gov/pubmed/24046624 http://dx.doi.org/10.1107/S160053681301547X |
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author | Mabkhot, Yahia Nasser Alatibi, Fatima Barakat, Assem Choudhary, M. Iqbal Yousuf, Sammer |
author_facet | Mabkhot, Yahia Nasser Alatibi, Fatima Barakat, Assem Choudhary, M. Iqbal Yousuf, Sammer |
author_sort | Mabkhot, Yahia Nasser |
collection | PubMed |
description | In the title compound, C(16)H(17)NO(3)S, a thiophene derivative with amino phenyl, acetyl, methyl and ethyl carboxyl susbtituents attached to a central thiophene ring, the phenyl and thiophene rings form a dihedral angle of 36.92 (9) Å. The molecular conformation is stabilized by an intramolecular N—H⋯O hydrogen bond, which forms an S(6) ring motif. |
format | Online Article Text |
id | pubmed-3772481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-37724812013-09-17 Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate Mabkhot, Yahia Nasser Alatibi, Fatima Barakat, Assem Choudhary, M. Iqbal Yousuf, Sammer Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(17)NO(3)S, a thiophene derivative with amino phenyl, acetyl, methyl and ethyl carboxyl susbtituents attached to a central thiophene ring, the phenyl and thiophene rings form a dihedral angle of 36.92 (9) Å. The molecular conformation is stabilized by an intramolecular N—H⋯O hydrogen bond, which forms an S(6) ring motif. International Union of Crystallography 2013-06-08 /pmc/articles/PMC3772481/ /pubmed/24046624 http://dx.doi.org/10.1107/S160053681301547X Text en © Mabkhot 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 Mabkhot, Yahia Nasser Alatibi, Fatima Barakat, Assem Choudhary, M. Iqbal Yousuf, Sammer Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title | Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title_full | Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title_fullStr | Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title_full_unstemmed | Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title_short | Ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
title_sort | ethyl 4-acetyl-5-anilino-3-methylthiophene-2-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772481/ https://www.ncbi.nlm.nih.gov/pubmed/24046624 http://dx.doi.org/10.1107/S160053681301547X |
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