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3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one
In the title compound, C(16)H(15)N(3)O, the dihedral angle between the indole ring system (r.m.s. deviation = 0.020 Å) and the phenyl ring is 14.49 (9)°. The molecular conformation is supported by an intramolecular C—H⋯O interaction, which closes an S(7) ring. In the crystal, inversion dimers lin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589046/ https://www.ncbi.nlm.nih.gov/pubmed/23476282 http://dx.doi.org/10.1107/S1600536812047988 |
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author | Ashiq, Uzma Jamal, Rifat Ara Ismail, Hina Khan, Khalid Mohammed Yousuf, Sammer |
author_facet | Ashiq, Uzma Jamal, Rifat Ara Ismail, Hina Khan, Khalid Mohammed Yousuf, Sammer |
author_sort | Ashiq, Uzma |
collection | PubMed |
description | In the title compound, C(16)H(15)N(3)O, the dihedral angle between the indole ring system (r.m.s. deviation = 0.020 Å) and the phenyl ring is 14.49 (9)°. The molecular conformation is supported by an intramolecular C—H⋯O interaction, which closes an S(7) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops. |
format | Online Article Text |
id | pubmed-3589046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35890462013-03-08 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one Ashiq, Uzma Jamal, Rifat Ara Ismail, Hina Khan, Khalid Mohammed Yousuf, Sammer Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(15)N(3)O, the dihedral angle between the indole ring system (r.m.s. deviation = 0.020 Å) and the phenyl ring is 14.49 (9)°. The molecular conformation is supported by an intramolecular C—H⋯O interaction, which closes an S(7) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2012-11-28 /pmc/articles/PMC3589046/ /pubmed/23476282 http://dx.doi.org/10.1107/S1600536812047988 Text en © Ashiq et al. 2012 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 Ashiq, Uzma Jamal, Rifat Ara Ismail, Hina Khan, Khalid Mohammed Yousuf, Sammer 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title | 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title_full | 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title_fullStr | 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title_full_unstemmed | 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title_short | 3-(2-Ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
title_sort | 3-(2-ethyl-2-phenylhydrazin-1-ylidene)indolin-2-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589046/ https://www.ncbi.nlm.nih.gov/pubmed/23476282 http://dx.doi.org/10.1107/S1600536812047988 |
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