The asymmetric unit of the title compound, C~14~H~13~N~3~O~3~·H~2~O, contains one molecule of __N__′-(4-hydroxy-3-methoxybenzylidene)isonicotinohydrazide and one solvent water molecule. The crystal packing is stabilized by O—H...N and O—H...O hydrogen bonds.
(E)-N'-(3-Hydroxy-4-methoxybenzylidene)isonicotinohydrazide
✍ Scribed by Shi, Jun
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 131 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
The title compound, C 16 H 16 N 2 O 4 , was synthesized by the reaction of 3-hydroxy-4-methoxybenzaldehyde with hydrazine hydrate. The molecule possesses a crystallographically imposed centre of symmetry. An intramolecular O-HÁ Á ÁO hydrogen bond promotes planarity of the molecular backbone. In the
The title compound, C 21 H 19 N 3 O 3 , was prepared by the reaction of 4-benzyloxy-3-methoxybenzaldehyde and isonicotinohydrazide. The vanillin group makes dihedral angles of 27.88 (7) and 58.94 (6) with the planes of the pyridine and phenyl rings, respectively. A weak intermolecular C-HÁ Á ÁN hydr
In the title compound, C 16 H 16 N 2 O 4 Á0.5CH 3 CH 2 OH, the Schiff base is approximately planar. An intramolecular N-HÁ Á ÁO hydrogen bond stabilizes the molecular structure. The molecules are linked by O-HÁ Á ÁO hydrogen bonds to form a chain along the b axis.