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Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate

In the title 1,2,4-oxadiazole derivative, C(19)H(18)ClN(3)O(3), the 1,2,4-oxadiazole ring makes dihedral angles of 12.83 (8) and 4.89 (8)°, respectively, with the benzyl and 4-chloro­phenyl rings, while the dihedral angle between the benzyl and 4-chloro­phenyl rings is 11.53 (7)°. In the crystal, mo...

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Autores principales: Fun, Hoong-Kun, Sumangala, V., Nagaraja, G. K., Poojary, Boja, Chantrapromma, Suchada
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051527/
https://www.ncbi.nlm.nih.gov/pubmed/21523090
http://dx.doi.org/10.1107/S1600536811001504
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author Fun, Hoong-Kun
Sumangala, V.
Nagaraja, G. K.
Poojary, Boja
Chantrapromma, Suchada
author_facet Fun, Hoong-Kun
Sumangala, V.
Nagaraja, G. K.
Poojary, Boja
Chantrapromma, Suchada
author_sort Fun, Hoong-Kun
collection PubMed
description In the title 1,2,4-oxadiazole derivative, C(19)H(18)ClN(3)O(3), the 1,2,4-oxadiazole ring makes dihedral angles of 12.83 (8) and 4.89 (8)°, respectively, with the benzyl and 4-chloro­phenyl rings, while the dihedral angle between the benzyl and 4-chloro­phenyl rings is 11.53 (7)°. In the crystal, mol­ecules are linked by N—H⋯N hydrogen bonds into helical chains along the b axis. A weak C—H⋯π inter­action is also present.
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spelling pubmed-30515272011-04-26 Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate Fun, Hoong-Kun Sumangala, V. Nagaraja, G. K. Poojary, Boja Chantrapromma, Suchada Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title 1,2,4-oxadiazole derivative, C(19)H(18)ClN(3)O(3), the 1,2,4-oxadiazole ring makes dihedral angles of 12.83 (8) and 4.89 (8)°, respectively, with the benzyl and 4-chloro­phenyl rings, while the dihedral angle between the benzyl and 4-chloro­phenyl rings is 11.53 (7)°. In the crystal, mol­ecules are linked by N—H⋯N hydrogen bonds into helical chains along the b axis. A weak C—H⋯π inter­action is also present. International Union of Crystallography 2011-01-15 /pmc/articles/PMC3051527/ /pubmed/21523090 http://dx.doi.org/10.1107/S1600536811001504 Text en © Fun et al. 2011 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
Fun, Hoong-Kun
Sumangala, V.
Nagaraja, G. K.
Poojary, Boja
Chantrapromma, Suchada
Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title_full Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title_fullStr Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title_full_unstemmed Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title_short Benzyl N-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
title_sort benzyl n-{2-[5-(4-chloro­phen­yl)-1,2,4-oxadiazol-3-yl]propan-2-yl}carbamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051527/
https://www.ncbi.nlm.nih.gov/pubmed/21523090
http://dx.doi.org/10.1107/S1600536811001504
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