Cargando…

2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide

In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thia­zole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops....

Descripción completa

Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Nayak, Prakash S., Narayana, B., Sarojini, B. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414920/
https://www.ncbi.nlm.nih.gov/pubmed/22904907
http://dx.doi.org/10.1107/S1600536812031583
_version_ 1782240279484432384
author Fun, Hoong-Kun
Quah, Ching Kheng
Nayak, Prakash S.
Narayana, B.
Sarojini, B. K.
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Nayak, Prakash S.
Narayana, B.
Sarojini, B. K.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thia­zole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The dimers are linked by C—H⋯O hydrogen bonds into chains propagating along [110].
format Online
Article
Text
id pubmed-3414920
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-34149202012-08-17 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide Fun, Hoong-Kun Quah, Ching Kheng Nayak, Prakash S. Narayana, B. Sarojini, B. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thia­zole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The dimers are linked by C—H⋯O hydrogen bonds into chains propagating along [110]. International Union of Crystallography 2012-07-18 /pmc/articles/PMC3414920/ /pubmed/22904907 http://dx.doi.org/10.1107/S1600536812031583 Text en © Fun 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
Fun, Hoong-Kun
Quah, Ching Kheng
Nayak, Prakash S.
Narayana, B.
Sarojini, B. K.
2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title_full 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title_fullStr 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title_full_unstemmed 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title_short 2-(Naphthalen-1-yl)-N-(1,3-thia­zol-2-yl)acetamide
title_sort 2-(naphthalen-1-yl)-n-(1,3-thia­zol-2-yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414920/
https://www.ncbi.nlm.nih.gov/pubmed/22904907
http://dx.doi.org/10.1107/S1600536812031583
work_keys_str_mv AT funhoongkun 2naphthalen1yln13thiazol2ylacetamide
AT quahchingkheng 2naphthalen1yln13thiazol2ylacetamide
AT nayakprakashs 2naphthalen1yln13thiazol2ylacetamide
AT narayanab 2naphthalen1yln13thiazol2ylacetamide
AT sarojinibk 2naphthalen1yln13thiazol2ylacetamide