Solubility of Thiophene-, Furan- and Pyrrole-2-Carboxaldehyde Phenylhydrazone Derivatives in 2.82 mol⋅L−1 Aqueous DMSO at 298.15 K, Inhibition of Lymphoproliferation and Tubulin Polymerization: A Study Based on the Scaled Particle Theory

Volume-related properties of thiophene and furan-2-carboxaldehyde phenylhydrazone derivatives in DMSO: A discussion about non-intrinsic contribution

“…It was shown that the transfer of several phenylhydrazone derivatives from water to 2.82 M aqueous DMSO at 298.15 K is a spontaneous process [1]. The high solubility of these derivatives in aqueous DMSO with respect to pure water was explained based on the difference in the work of cavity creation associated with the transfer of each solute from water to DMSO-water binary mixture, and this quantity is the dominant factor in the magnitude of standard Gibbs energy.…”

Estimation of ground and excited states dipole moments of α-hydroxy phenyl hydrazone derivatives: Experimental and quantum chemical methods

“…Therefore, research on solute-solvent specific and non-specific interactions affords to understand the binding of a compound with target substrate [1][2][3][4][5][6][7][8]. Nevertheless, chemical process of hydrazone compounds in solution is rarely investigated [6,7,9,10].…”