3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one

In the title compound, C(9)H(10)N(2)OS, the thienopyrimidine ring system is almost planar [greatest deviation from the mean plane = 0.0318 (13) Å for the S atom]. The crystal packing features C—H⋯O hydrogen bonds and π–π stacking inter­actions between inversion-related pairs of mol­ecules with a cen...

Descripción completa

Detalles Bibliográficos
Autores principales: Khatamov, Khamroqul, Saitqulov, Fozil, Ashurov, Jamshid, Shakhidoyatov, Khusnutdin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435752/
https://www.ncbi.nlm.nih.gov/pubmed/22969623
http://dx.doi.org/10.1107/S1600536812035416
_version_ 1782242584575344640
author Khatamov, Khamroqul
Saitqulov, Fozil
Ashurov, Jamshid
Shakhidoyatov, Khusnutdin
author_facet Khatamov, Khamroqul
Saitqulov, Fozil
Ashurov, Jamshid
Shakhidoyatov, Khusnutdin
author_sort Khatamov, Khamroqul
collection PubMed
description In the title compound, C(9)H(10)N(2)OS, the thienopyrimidine ring system is almost planar [greatest deviation from the mean plane = 0.0318 (13) Å for the S atom]. The crystal packing features C—H⋯O hydrogen bonds and π–π stacking inter­actions between inversion-related pairs of mol­ecules with a centroid–centroid distance of 3.530 (3) Å.
format Online
Article
Text
id pubmed-3435752
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-34357522012-09-11 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one Khatamov, Khamroqul Saitqulov, Fozil Ashurov, Jamshid Shakhidoyatov, Khusnutdin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(9)H(10)N(2)OS, the thienopyrimidine ring system is almost planar [greatest deviation from the mean plane = 0.0318 (13) Å for the S atom]. The crystal packing features C—H⋯O hydrogen bonds and π–π stacking inter­actions between inversion-related pairs of mol­ecules with a centroid–centroid distance of 3.530 (3) Å. International Union of Crystallography 2012-08-23 /pmc/articles/PMC3435752/ /pubmed/22969623 http://dx.doi.org/10.1107/S1600536812035416 Text en © Khatamov 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
Khatamov, Khamroqul
Saitqulov, Fozil
Ashurov, Jamshid
Shakhidoyatov, Khusnutdin
3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title_full 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title_fullStr 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title_full_unstemmed 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title_short 3,5,6-Trimethyl­thieno[2,3-d]pyrimidin-4(3H)-one
title_sort 3,5,6-trimethyl­thieno[2,3-d]pyrimidin-4(3h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435752/
https://www.ncbi.nlm.nih.gov/pubmed/22969623
http://dx.doi.org/10.1107/S1600536812035416
work_keys_str_mv AT khatamovkhamroqul 356trimethylthieno23dpyrimidin43hone
AT saitqulovfozil 356trimethylthieno23dpyrimidin43hone
AT ashurovjamshid 356trimethylthieno23dpyrimidin43hone
AT shakhidoyatovkhusnutdin 356trimethylthieno23dpyrimidin43hone

Ejemplares similares