2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide
In the title compound, C15H12N2OS, 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) &am...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
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?S1600536812031583 |
| _version_ | 1818997500983377920 |
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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, C15H12N2OS, 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 R22(8) loops. The dimers are linked by C—H...O hydrogen bonds into chains propagating along [110]. |
| first_indexed | 2024-12-20T21:46:38Z |
| format | Article |
| id | doaj.art-30f0fa91c4b5437d9b792a19a7d7e611 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-20T21:46:38Z |
| publishDate | 2012-08-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-30f0fa91c4b5437d9b792a19a7d7e6112022-12-21T19:25:40ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-08-01688o2464o246410.1107/S16005368120315832-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamideHoong-Kun FunChing Kheng QuahPrakash S. NayakB. NarayanaB. K. SarojiniIn the title compound, C15H12N2OS, 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 R22(8) loops. The dimers are linked by C—H...O hydrogen bonds into chains propagating along [110].http://scripts.iucr.org/cgi-bin/paper?S1600536812031583 |
| spellingShingle | Hoong-Kun Fun Ching Kheng Quah Prakash S. Nayak B. Narayana B. K. Sarojini 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide Acta Crystallographica Section E |
| 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 |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536812031583 |
| work_keys_str_mv | AT hoongkunfun 2naphthalen1yln13thiazol2ylacetamide AT chingkhengquah 2naphthalen1yln13thiazol2ylacetamide AT prakashsnayak 2naphthalen1yln13thiazol2ylacetamide AT bnarayana 2naphthalen1yln13thiazol2ylacetamide AT bksarojini 2naphthalen1yln13thiazol2ylacetamide |