Cargando…
1-Benzyloxy-1H-benzotriazole
In the title compound, C(13)H(11)N(3)O, the dihedral angle between the benzotriazole ring system [maximum deviation = 0.027 (16) Å] and the benzene ring is 10.28 (9)°. The C—C—O—N bond adopts an anti conformation [torsion angle = −177.11 (16)°]. In the crystal, the molecules interact via weak C—H⋯...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394030/ https://www.ncbi.nlm.nih.gov/pubmed/22798895 http://dx.doi.org/10.1107/S1600536812028395 |
_version_ | 1782237807303983104 |
---|---|
author | Jebas, Samuel Robinson Selvarathy Grace, P. Ravindran Durai Nayagam, B. Schollmeyer, Dieter |
author_facet | Jebas, Samuel Robinson Selvarathy Grace, P. Ravindran Durai Nayagam, B. Schollmeyer, Dieter |
author_sort | Jebas, Samuel Robinson |
collection | PubMed |
description | In the title compound, C(13)H(11)N(3)O, the dihedral angle between the benzotriazole ring system [maximum deviation = 0.027 (16) Å] and the benzene ring is 10.28 (9)°. The C—C—O—N bond adopts an anti conformation [torsion angle = −177.11 (16)°]. In the crystal, the molecules interact via weak C—H⋯π interactions and aromatic π–π stacking [centroid-to-centroid distance = 3.731 (12) Å]. |
format | Online Article Text |
id | pubmed-3394030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33940302012-07-13 1-Benzyloxy-1H-benzotriazole Jebas, Samuel Robinson Selvarathy Grace, P. Ravindran Durai Nayagam, B. Schollmeyer, Dieter Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(11)N(3)O, the dihedral angle between the benzotriazole ring system [maximum deviation = 0.027 (16) Å] and the benzene ring is 10.28 (9)°. The C—C—O—N bond adopts an anti conformation [torsion angle = −177.11 (16)°]. In the crystal, the molecules interact via weak C—H⋯π interactions and aromatic π–π stacking [centroid-to-centroid distance = 3.731 (12) Å]. International Union of Crystallography 2012-06-30 /pmc/articles/PMC3394030/ /pubmed/22798895 http://dx.doi.org/10.1107/S1600536812028395 Text en © Jebas 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 Jebas, Samuel Robinson Selvarathy Grace, P. Ravindran Durai Nayagam, B. Schollmeyer, Dieter 1-Benzyloxy-1H-benzotriazole |
title | 1-Benzyloxy-1H-benzotriazole |
title_full | 1-Benzyloxy-1H-benzotriazole |
title_fullStr | 1-Benzyloxy-1H-benzotriazole |
title_full_unstemmed | 1-Benzyloxy-1H-benzotriazole |
title_short | 1-Benzyloxy-1H-benzotriazole |
title_sort | 1-benzyloxy-1h-benzotriazole |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394030/ https://www.ncbi.nlm.nih.gov/pubmed/22798895 http://dx.doi.org/10.1107/S1600536812028395 |
work_keys_str_mv | AT jebassamuelrobinson 1benzyloxy1hbenzotriazole AT selvarathygracep 1benzyloxy1hbenzotriazole AT ravindrandurainayagamb 1benzyloxy1hbenzotriazole AT schollmeyerdieter 1benzyloxy1hbenzotriazole |