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Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate

The asymmetric unit of the title compound, C(9)H(7)N(3)O(2), is composed of two independent mol­ecules. The crystal structure is stabilized by C—H⋯O and C—H⋯N hydrogen bonds, forming a three-dimensional network. The crystal structure also features pyrazine–pyrazine π–π inter­actions [centroid–centro...

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Autores principales: Fun, Hoong-Kun, Hemamalini, Madhukar, Hazra, Anita, Goswami, Shyamaprosad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247504/
https://www.ncbi.nlm.nih.gov/pubmed/22220122
http://dx.doi.org/10.1107/S1600536811044412
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author Fun, Hoong-Kun
Hemamalini, Madhukar
Hazra, Anita
Goswami, Shyamaprosad
author_facet Fun, Hoong-Kun
Hemamalini, Madhukar
Hazra, Anita
Goswami, Shyamaprosad
author_sort Fun, Hoong-Kun
collection PubMed
description The asymmetric unit of the title compound, C(9)H(7)N(3)O(2), is composed of two independent mol­ecules. The crystal structure is stabilized by C—H⋯O and C—H⋯N hydrogen bonds, forming a three-dimensional network. The crystal structure also features pyrazine–pyrazine π–π inter­actions [centroid–centroid distance = 3.6994 (5) Å] and also pyridine–pyrazine π–π inter­actions [centroid–centroid distance = 3.6374 (5) Å].
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spelling pubmed-32475042012-01-04 Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate Fun, Hoong-Kun Hemamalini, Madhukar Hazra, Anita Goswami, Shyamaprosad Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(9)H(7)N(3)O(2), is composed of two independent mol­ecules. The crystal structure is stabilized by C—H⋯O and C—H⋯N hydrogen bonds, forming a three-dimensional network. The crystal structure also features pyrazine–pyrazine π–π inter­actions [centroid–centroid distance = 3.6994 (5) Å] and also pyridine–pyrazine π–π inter­actions [centroid–centroid distance = 3.6374 (5) Å]. International Union of Crystallography 2011-10-29 /pmc/articles/PMC3247504/ /pubmed/22220122 http://dx.doi.org/10.1107/S1600536811044412 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
Hemamalini, Madhukar
Hazra, Anita
Goswami, Shyamaprosad
Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title_full Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title_fullStr Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title_full_unstemmed Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title_short Methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
title_sort methyl pyrido[2,3-b]pyrazine-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247504/
https://www.ncbi.nlm.nih.gov/pubmed/22220122
http://dx.doi.org/10.1107/S1600536811044412
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AT hemamalinimadhukar methylpyrido23bpyrazine3carboxylate
AT hazraanita methylpyrido23bpyrazine3carboxylate
AT goswamishyamaprosad methylpyrido23bpyrazine3carboxylate