Related Experiment Video
Updated: May 27, 2026

Preparation of Contiguous Bisaziridines for Regioselective Ring-Opening Reactions
Published on: July 28, 2022
1,5-Bis(4-meth-oxy-benzyl-idene)thio-carbonohydrazide methanol monosolvate
1School of Petrochemical Engineering, Shenyang University of Technology, Liaoyang 111003, People's Republic of China.
Abstract:
In the title compound, C(17)H(18)N(4)O(2)S·CH(3)OH, the two benzene rings in the thio-carbonohydrazide mol-ecule form a dihedral angle of 22.42 (18)°. Pairs of N-H⋯S hydrogen bonds link thio-carbonohydrazide mol-ecules into centrosymmetric dimers. Methanol solvent mol-ecules serve as donors (O-H⋯S and O-H⋯N) and acceptors (N-H⋯O and C-H⋯O) of weak inter-molecular hydrogen bonds, which link further these dimers into double ribbons along the b axis.
More Related Videos
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Preparation and Reactions of Sulfides
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Multiple Halogenation of Methyl Ketones: Haloform Reaction
Formation of Halohydrin from Alkenes
Hydroboration-Oxidation of Alkenes

