In the title compound, C 16 H 15 N 3 OS, molecules form inversionrelated dimers via N-HÁ Á ÁS hydrogen bonds. The structure is further stabilized by intermolecularstacking interactions down the a axis.
Tautomerism in 3-ethoxy-5-phenyl-1,2,4-triazole
✍ Scribed by William M. Litchman
- Book ID
- 112126884
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1982
- Tongue
- English
- Weight
- 124 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-152X
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📜 SIMILAR VOLUMES
## Abstract The non‐degenerate tautomers of 3‐nitro‐1,2,4‐triazole‐5‐one (NTO) radical anions were investigated for the first time by an ESR method during electrochemical reduction of NTO in an aprotic medium. Copyright © 2009 John Wiley & Sons, Ltd.
## Abstract Die Aldehyde **7**, erste Vertreter der noch unbekannten Klasse 1‐substituierter 1,2,4‐Triazol‐5‐carbaldehyde, sind in sehr guter Ausbeute durch Bleitetraacetatoxidation der Alkohole **2** zugänglich; ein alternativer Weg besteht in der Anwendung der Kröhnke‐Reaktion auf **5**. Als Folg
In the crystal structure of the title compound, C 15 H 14 N 4 , all three aromatic rings, viz. 1,2,4-triazole, pyridine and benzene. The crystal structure shows that all three rings are not coplanar.
In the title compound, C 20 H 17 N 5 O, the two pyridyl rings form dihedral angles of 30.0 (1) and 21.0 (1) with the triazole ring, and the dihedral angle between the triazole and benzene rings is 71.4 (1) . The crystal packing is stabilized by C-HÁ Á ÁN hydrogen bonds.