The knowledge of solubility and solution thermodynamics for 1-(3-nitrophenyl)ethanone and 1-(4-nitrophenyl)ethenone in different solvents is essential for their purification and further theoretical study. In this work, the solid−liquid equilibrium for 1-(3-nitrophenyl)ethanone and 1-(4-nitrophenyl)ethenone in nine pure solvents (methanol, ethanol, n-propanol, isopropanol, acetone, acetonitrile, ethyl acetate, toluene, and cyclohexane) was established with the isothermal saturation method at temperatures T = (278.15 to 318.15) K under pressure of 101.2 kPa. The mole fraction solubility of 1-(3-nitrophenyl)ethanone obeys the following order from high to low in different solvents: acetone > acetonitrile, ethyl acetate > toluene > methanol > ethanol > n-propanol, isopropanol > cyclohexane. While in 1-(4-nitrophenyl)ethanone + solvents, the order of the data from high to low is acetone > acetonitrile > ethyl acetate > toluene > methanol > ethanol > n-propanol > isopropanol > cyclohexane. The modified Apelblat equation, λh equation, Wilson model, and nonrandom two-liquid model were employed to correlate the measured solubility data of 1-(3-nitrophenyl)ethanone and 1-(4-nitrophenyl)ethanone in the selected solvents. Results showed that the largest values of relative average deviation and root-mean-square deviation obtained with the four models were no greater than 2.78% and 7.59 × 10 −3 , respectively. The modified Apelblat equation provided better results than the other three models. Furthermore, the mixing properties, including Gibbs energy, mixing enthalpy, mixing entropy, activity coefficient at infinitesimal concentration (γ 1 ∞ ), and reduced excess enthalpy (H 1 E,∞ ) were computed. The mixing processes of 1-(3-nitrophenyl)ethanone and 1-(4-nitrophenyl)ethenone in the studied solvents are all spontaneous and endothermic. The obtained solubility and thermodynamic studies are very helpful for optimizing the purification process of 1-(3-nitrophenyl)ethanone and 1-(4-nitrophenyl)ethenone.