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2,7-Bis(trichloromethyl)-1,8-naphthyridine
The complete molecule of the title compound, C(10)H(4)Cl(6)N(2), is generated by crystallographic twofold symmetry, with two C atoms lying on the rotation axis; the 1,8-naphthyridine ring is almost planar with an r.m.s. deviation of 0.0002 Å. In the crystal structure, the molecules are stacked in...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983609/ https://www.ncbi.nlm.nih.gov/pubmed/21580380 http://dx.doi.org/10.1107/S1600536810005234 |
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author | Fun, Hoong-Kun Chantrapromma, Suchada Maity, Annada C. Goswami, Shyamaprosad |
author_facet | Fun, Hoong-Kun Chantrapromma, Suchada Maity, Annada C. Goswami, Shyamaprosad |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | The complete molecule of the title compound, C(10)H(4)Cl(6)N(2), is generated by crystallographic twofold symmetry, with two C atoms lying on the rotation axis; the 1,8-naphthyridine ring is almost planar with an r.m.s. deviation of 0.0002 Å. In the crystal structure, the molecules are stacked in an antiparallel manner along [001]. Short Cl⋯Cl [3.3502 (4)] and Cl⋯N [3.2004 (11)–3.2220 (10) Å] contacts are observed in the crystal structure. |
format | Text |
id | pubmed-2983609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29836092010-12-30 2,7-Bis(trichloromethyl)-1,8-naphthyridine Fun, Hoong-Kun Chantrapromma, Suchada Maity, Annada C. Goswami, Shyamaprosad Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule of the title compound, C(10)H(4)Cl(6)N(2), is generated by crystallographic twofold symmetry, with two C atoms lying on the rotation axis; the 1,8-naphthyridine ring is almost planar with an r.m.s. deviation of 0.0002 Å. In the crystal structure, the molecules are stacked in an antiparallel manner along [001]. Short Cl⋯Cl [3.3502 (4)] and Cl⋯N [3.2004 (11)–3.2220 (10) Å] contacts are observed in the crystal structure. International Union of Crystallography 2010-02-13 /pmc/articles/PMC2983609/ /pubmed/21580380 http://dx.doi.org/10.1107/S1600536810005234 Text en © Fun 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 Fun, Hoong-Kun Chantrapromma, Suchada Maity, Annada C. Goswami, Shyamaprosad 2,7-Bis(trichloromethyl)-1,8-naphthyridine |
title | 2,7-Bis(trichloromethyl)-1,8-naphthyridine
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title_full | 2,7-Bis(trichloromethyl)-1,8-naphthyridine
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title_fullStr | 2,7-Bis(trichloromethyl)-1,8-naphthyridine
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title_full_unstemmed | 2,7-Bis(trichloromethyl)-1,8-naphthyridine
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title_short | 2,7-Bis(trichloromethyl)-1,8-naphthyridine
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title_sort | 2,7-bis(trichloromethyl)-1,8-naphthyridine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983609/ https://www.ncbi.nlm.nih.gov/pubmed/21580380 http://dx.doi.org/10.1107/S1600536810005234 |
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