Nifedipine–pyrazine (2/1)
In the title compound, 2C17H18N2O6·C4H4N2 [systematic name: 3,5-dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate–pyrazine (2/1)], the complete pyrazine molecule is generated by crystallographic inversion symmetry. The center of the pyrazine rin...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2010-09-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810031703 |
| _version_ | 1819105531628879872 |
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| author | Nate Schultheiss Melanie Roe Jared P. Smit |
| author_facet | Nate Schultheiss Melanie Roe Jared P. Smit |
| author_sort | Nate Schultheiss |
| collection | DOAJ |
| description | In the title compound, 2C17H18N2O6·C4H4N2 [systematic name: 3,5-dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate–pyrazine (2/1)], the complete pyrazine molecule is generated by crystallographic inversion symmetry. The center of the pyrazine ring lies on an inversion center. The nifedipine molecules are linked into chains along the c axis through N—H...O hydrogen bonds, while the pyrazine molecules are organized in the structure through van der Waals interactions. |
| first_indexed | 2024-12-22T02:23:44Z |
| format | Article |
| id | doaj.art-f0228d3ccb174da2917e81031e2bf25e |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-22T02:23:44Z |
| publishDate | 2010-09-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-f0228d3ccb174da2917e81031e2bf25e2022-12-21T18:42:03ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-09-01669o2297o229810.1107/S1600536810031703Nifedipine–pyrazine (2/1)Nate SchultheissMelanie RoeJared P. SmitIn the title compound, 2C17H18N2O6·C4H4N2 [systematic name: 3,5-dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate–pyrazine (2/1)], the complete pyrazine molecule is generated by crystallographic inversion symmetry. The center of the pyrazine ring lies on an inversion center. The nifedipine molecules are linked into chains along the c axis through N—H...O hydrogen bonds, while the pyrazine molecules are organized in the structure through van der Waals interactions.http://scripts.iucr.org/cgi-bin/paper?S1600536810031703 |
| spellingShingle | Nate Schultheiss Melanie Roe Jared P. Smit Nifedipine–pyrazine (2/1) Acta Crystallographica Section E |
| title | Nifedipine–pyrazine (2/1) |
| title_full | Nifedipine–pyrazine (2/1) |
| title_fullStr | Nifedipine–pyrazine (2/1) |
| title_full_unstemmed | Nifedipine–pyrazine (2/1) |
| title_short | Nifedipine–pyrazine (2/1) |
| title_sort | nifedipine amp 8211 pyrazine 2 1 |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536810031703 |
| work_keys_str_mv | AT nateschultheiss nifedipineamp8211pyrazine21 AT melanieroe nifedipineamp8211pyrazine21 AT jaredpsmit nifedipineamp8211pyrazine21 |