3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)

The asymmetric unit of the title compound, C(18)H(18)Cl(2)N(2)O(2), contains one half of an independent mol­ecule, the other half being generated via a centre of inversion at the mol­ecular centroid. In the crystal structure, mol­ecular chains are formed through non-classical C—H⋯ O hydrogen bonds b...

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Detalles Bibliográficos
Autores principales: Rivera, Augusto, Rojas, Jicli José, Ríos-Motta, Jaime, Dušek, Michal, Fejfarová, Karla
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979041/
https://www.ncbi.nlm.nih.gov/pubmed/21579183
http://dx.doi.org/10.1107/S1600536810014248
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author Rivera, Augusto
Rojas, Jicli José
Ríos-Motta, Jaime
Dušek, Michal
Fejfarová, Karla
author_facet Rivera, Augusto
Rojas, Jicli José
Ríos-Motta, Jaime
Dušek, Michal
Fejfarová, Karla
author_sort Rivera, Augusto
collection PubMed
description The asymmetric unit of the title compound, C(18)H(18)Cl(2)N(2)O(2), contains one half of an independent mol­ecule, the other half being generated via a centre of inversion at the mol­ecular centroid. In the crystal structure, mol­ecular chains are formed through non-classical C—H⋯ O hydrogen bonds between an axial H atom of the oxazine ring and the O atom of a neighbouring mol­ecule.
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spelling pubmed-29790412010-12-30 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine) Rivera, Augusto Rojas, Jicli José Ríos-Motta, Jaime Dušek, Michal Fejfarová, Karla Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(18)H(18)Cl(2)N(2)O(2), contains one half of an independent mol­ecule, the other half being generated via a centre of inversion at the mol­ecular centroid. In the crystal structure, mol­ecular chains are formed through non-classical C—H⋯ O hydrogen bonds between an axial H atom of the oxazine ring and the O atom of a neighbouring mol­ecule. International Union of Crystallography 2010-04-21 /pmc/articles/PMC2979041/ /pubmed/21579183 http://dx.doi.org/10.1107/S1600536810014248 Text en © Rivera et al. 2010 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
Rivera, Augusto
Rojas, Jicli José
Ríos-Motta, Jaime
Dušek, Michal
Fejfarová, Karla
3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title_full 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title_fullStr 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title_full_unstemmed 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title_short 3,3′-Ethyl­enebis(3,4-dihydro-6-chloro-2H-1,3-benzoxazine)
title_sort 3,3′-ethyl­enebis(3,4-dihydro-6-chloro-2h-1,3-benzoxazine)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979041/
https://www.ncbi.nlm.nih.gov/pubmed/21579183
http://dx.doi.org/10.1107/S1600536810014248
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AT dusekmichal 33ethylenebis34dihydro6chloro2h13benzoxazine
AT fejfarovakarla 33ethylenebis34dihydro6chloro2h13benzoxazine

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