N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide
In the title compound, C14H16N2OS, the thiazole ring is essentially planar (r.m.s. deviation = 0.005 Å) and it forms a dihedral angle of 75.21 (8)° with the benzene ring. In the crystal, molecules are linked into inversion dimers by pairs of N&am...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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International Union of Crystallography
2012-08-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812031595 |
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author | Hoong-Kun Fun Ching Kheng Quah Prakash S. Nayak B. Narayana B. K. Sarojini |
author_facet | Hoong-Kun Fun Ching Kheng Quah Prakash S. Nayak B. Narayana B. K. Sarojini |
author_sort | Hoong-Kun Fun |
collection | DOAJ |
description | In the title compound, C14H16N2OS, the thiazole ring is essentially planar (r.m.s. deviation = 0.005 Å) and it forms a dihedral angle of 75.21 (8)° with the benzene ring. In the crystal, molecules are linked into inversion dimers by pairs of N—H...N hydrogen bonds to generate R22(8) loops. |
first_indexed | 2024-12-22T07:34:02Z |
format | Article |
id | doaj.art-d4ff20ef8f244d9e8d22fe48b1b8d3c3 |
institution | Directory Open Access Journal |
issn | 1600-5368 |
language | English |
last_indexed | 2024-12-22T07:34:02Z |
publishDate | 2012-08-01 |
publisher | International Union of Crystallography |
record_format | Article |
series | Acta Crystallographica Section E |
spelling | doaj.art-d4ff20ef8f244d9e8d22fe48b1b8d3c32022-12-21T18:33:56ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-08-01688o2461o246110.1107/S1600536812031595N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamideHoong-Kun FunChing Kheng QuahPrakash S. NayakB. NarayanaB. K. SarojiniIn the title compound, C14H16N2OS, the thiazole ring is essentially planar (r.m.s. deviation = 0.005 Å) and it forms a dihedral angle of 75.21 (8)° with the benzene ring. In the crystal, molecules are linked into inversion dimers by pairs of N—H...N hydrogen bonds to generate R22(8) loops.http://scripts.iucr.org/cgi-bin/paper?S1600536812031595 |
spellingShingle | Hoong-Kun Fun Ching Kheng Quah Prakash S. Nayak B. Narayana B. K. Sarojini N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide Acta Crystallographica Section E |
title | N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide |
title_full | N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide |
title_fullStr | N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide |
title_full_unstemmed | N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide |
title_short | N-(1,3-Thiazol-2-yl)-2-(2,4,6-trimethylphenyl)acetamide |
title_sort | n 1 3 thiazol 2 yl 2 2 4 6 trimethylphenyl acetamide |
url | http://scripts.iucr.org/cgi-bin/paper?S1600536812031595 |
work_keys_str_mv | AT hoongkunfun n13thiazol2yl2246trimethylphenylacetamide AT chingkhengquah n13thiazol2yl2246trimethylphenylacetamide AT prakashsnayak n13thiazol2yl2246trimethylphenylacetamide AT bnarayana n13thiazol2yl2246trimethylphenylacetamide AT bksarojini n13thiazol2yl2246trimethylphenylacetamide |