The title compound, C 10 H 11 BrN 2 O, was prepared by the reaction of p-bromobenzaldehyde and propionylhydrazine. Centrosymmetric dimers are formed through N-HÁ Á ÁO hydrogen bonds.
3-(4-Methoxyphenyl)propanohydrazide
✍ Scribed by Qadeer, Ghulam ;Rama, Nasim Hasan ;Malik, Muhammad Azaad ;Raftery, James
- Book ID
- 104491087
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 810 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
The title compound, C 10 H 12 N 2 O 2 , is an important intermediate for the synthesis of biologically active heterocyclic compounds. The planar hydrazide group is oriented with respect to the benzene ring at a dihedral angle of 73.93 (3) . ## Related literature For general background, see:
In the title compound, C 17 H 16 O 3 , the dihedral angle between the benzene rings is 10.05 (9) . Intermolecular C-HÁ Á ÁO hydrogen bonds link the molecules to form chains along the b axis. The crystal structure is further stabilized by C-HÁ Á Á interactions.
In the structure of the title compound, C 16 H 16 N 2 O 2 S, the dihedral angle between the two aromatic ring planes is 48.3 (1) . Intermolecular N-HÁ Á ÁS hydrogen bonds link the molecules into dimers which are stacked along [100].
The crystal structure of the title compound, C~22~H~16~FNO~3~, is stablized by C—H...π intermolecular interactions.