(E)-N′-(4-Benzyloxy-3-methoxybenzylidene)isonicotinohydrazide
✍ Scribed by Shi, Jun
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 134 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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 hydrogen bond helps to consolidate the crystal packing.
📜 SIMILAR VOLUMES
In the title compound, C 20 H 16 ClN 3 O 2 , the central benzene ring makes dihedral angles of 68.91 (5) and 60.23 (5) with the chlorobenzene ring and the pyridine ring, respectively. The packing is stabilized by intermolecular N-HÁ Á ÁO hydrogen bonds and weak, non-classical intermolecular C-HÁ Á Á
An anhydrous ethanol solution of 4-benzyloxy-3-methoxybenzaldehyde (2.42 g, 10 mmol) was added to an anhydrous ethanol
In the title compound, C 21 H 18 N 4 O 5 , the central vanillin group makes dihedral angles of 8.76 (13) and 62.38 (6) with its attached pyridine and nitrobenzene rings, respectively. The crystal packing is stabilized by N-HÁ Á ÁN hydrogen bonds and C-HÁ Á ÁO interactions, leading to an infinite net
In the title compound, C 22 H 20 N 4 O 5 , the central vanillin group makes dihedral angles of 4.44 (11) and 60.33 (6) with the pyridine and other benzene rings. The crystal packing is stabilized by N-HÁ Á ÁN hydrogen bonds and C-HÁ Á ÁO interactions, leading to an infinite network.