2-(1H-indol-3-ylcarbon­yl)acetonitrile

The title compound, C(11)H(8)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit which are approximately perpendicular to each other [79.97 (6)°]. The indole ring system is planar [r.m.s. deviation = 0.010 (1) Å]. The crystal structure is stabilized by int...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramesh, P., Subbiahpandi, A., Thirumurugan, P., Perumal, Paramasivan T., Ponnuswamy, M. N.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968615/
https://www.ncbi.nlm.nih.gov/pubmed/21582120
http://dx.doi.org/10.1107/S1600536809001342
_version_ 1782189932494716928
author Ramesh, P.
Subbiahpandi, A.
Thirumurugan, P.
Perumal, Paramasivan T.
Ponnuswamy, M. N.
author_facet Ramesh, P.
Subbiahpandi, A.
Thirumurugan, P.
Perumal, Paramasivan T.
Ponnuswamy, M. N.
author_sort Ramesh, P.
collection PubMed
description The title compound, C(11)H(8)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit which are approximately perpendicular to each other [79.97 (6)°]. The indole ring system is planar [r.m.s. deviation = 0.010 (1) Å]. The crystal structure is stabilized by inter­molecular C—H⋯N and N—H⋯O inter­actions.
format Text
id pubmed-2968615
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29686152010-12-30 2-(1H-indol-3-ylcarbon­yl)acetonitrile Ramesh, P. Subbiahpandi, A. Thirumurugan, P. Perumal, Paramasivan T. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(8)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit which are approximately perpendicular to each other [79.97 (6)°]. The indole ring system is planar [r.m.s. deviation = 0.010 (1) Å]. The crystal structure is stabilized by inter­molecular C—H⋯N and N—H⋯O inter­actions. International Union of Crystallography 2009-02-04 /pmc/articles/PMC2968615/ /pubmed/21582120 http://dx.doi.org/10.1107/S1600536809001342 Text en © Ramesh et al. 2009 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
Ramesh, P.
Subbiahpandi, A.
Thirumurugan, P.
Perumal, Paramasivan T.
Ponnuswamy, M. N.
2-(1H-indol-3-ylcarbon­yl)acetonitrile
title 2-(1H-indol-3-ylcarbon­yl)acetonitrile
title_full 2-(1H-indol-3-ylcarbon­yl)acetonitrile
title_fullStr 2-(1H-indol-3-ylcarbon­yl)acetonitrile
title_full_unstemmed 2-(1H-indol-3-ylcarbon­yl)acetonitrile
title_short 2-(1H-indol-3-ylcarbon­yl)acetonitrile
title_sort 2-(1h-indol-3-ylcarbon­yl)acetonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968615/
https://www.ncbi.nlm.nih.gov/pubmed/21582120
http://dx.doi.org/10.1107/S1600536809001342
work_keys_str_mv AT rameshp 21hindol3ylcarbonylacetonitrile
AT subbiahpandia 21hindol3ylcarbonylacetonitrile
AT thirumuruganp 21hindol3ylcarbonylacetonitrile
AT perumalparamasivant 21hindol3ylcarbonylacetonitrile
AT ponnuswamymn 21hindol3ylcarbonylacetonitrile

Ejemplares similares