(E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone
In the title compound, C15H15N3OS, the thiosemicarbazone group adopts an E configuration with respect to the C N bond. The benzaldehyde thiosemicarbazone fragment is almost planar [maximum deviation = 0.012 (1) A ° ], while the dihedral angle between the benzyloxy and phenyl rings is 72.48 (5)....
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English English |
| Published: |
International Union of Crystallography
2008
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| Online Access: | http://psasir.upm.edu.my/id/eprint/6157/ http://psasir.upm.edu.my/id/eprint/6157/1/63.pdf |
| _version_ | 1848840299818778624 |
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| author | Tarafder, Md. Tofazzal Hossain Islam, M. A. A. A. A. Crouse, Karen Anne Chantrapromma, Suchada Fun, Hoong Kun |
| author_facet | Tarafder, Md. Tofazzal Hossain Islam, M. A. A. A. A. Crouse, Karen Anne Chantrapromma, Suchada Fun, Hoong Kun |
| author_sort | Tarafder, Md. Tofazzal Hossain |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | In the title compound, C15H15N3OS, the thiosemicarbazone
group adopts an E configuration with respect to the C N
bond. The benzaldehyde thiosemicarbazone fragment is
almost planar [maximum deviation = 0.012 (1) A ° ], while the dihedral angle between the benzyloxy and phenyl rings is
72.48 (5). In the crystal structure, molecules are interconnected by N—H N and N—H S hydrogen bonds,
forming a two-dimensional network parallel to the bc plane
and are further stacked along the a axis by – interactions
[centroid–centroid separation 3.9043 (7) A ° ]. The crystal structure is also stabilized by C—H interactions |
| first_indexed | 2025-11-15T07:25:09Z |
| format | Article |
| id | upm-6157 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English English |
| last_indexed | 2025-11-15T07:25:09Z |
| publishDate | 2008 |
| publisher | International Union of Crystallography |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-61572013-05-27T07:27:35Z http://psasir.upm.edu.my/id/eprint/6157/ (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone Tarafder, Md. Tofazzal Hossain Islam, M. A. A. A. A. Crouse, Karen Anne Chantrapromma, Suchada Fun, Hoong Kun In the title compound, C15H15N3OS, the thiosemicarbazone group adopts an E configuration with respect to the C N bond. The benzaldehyde thiosemicarbazone fragment is almost planar [maximum deviation = 0.012 (1) A ° ], while the dihedral angle between the benzyloxy and phenyl rings is 72.48 (5). In the crystal structure, molecules are interconnected by N—H N and N—H S hydrogen bonds, forming a two-dimensional network parallel to the bc plane and are further stacked along the a axis by – interactions [centroid–centroid separation 3.9043 (7) A ° ]. The crystal structure is also stabilized by C—H interactions International Union of Crystallography 2008 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/6157/1/63.pdf Tarafder, Md. Tofazzal Hossain and Islam, M. A. A. A. A. and Crouse, Karen Anne and Chantrapromma, Suchada and Fun, Hoong Kun (2008) (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone. Acta Crystallographica Section E: Structure Reports Online, 64 (6). pp. 988-989. ISSN 1600-5368 http://dx.doi.org/10.1107/S1600536808012671 10.1107/S1600536808012671 English |
| spellingShingle | Tarafder, Md. Tofazzal Hossain Islam, M. A. A. A. A. Crouse, Karen Anne Chantrapromma, Suchada Fun, Hoong Kun (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title | (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title_full | (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title_fullStr | (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title_full_unstemmed | (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title_short | (E)-4-(Benzyloxy)Benzaldehyde Thiosemicarbazone |
| title_sort | (e)-4-(benzyloxy)benzaldehyde thiosemicarbazone |
| url | http://psasir.upm.edu.my/id/eprint/6157/ http://psasir.upm.edu.my/id/eprint/6157/ http://psasir.upm.edu.my/id/eprint/6157/ http://psasir.upm.edu.my/id/eprint/6157/1/63.pdf |