Barbituric acid is a heterocyclic compound with various pharmacological and biological applications. This review paper provides a comprehensive overview of barbituric acid’s synthesis, reactions, and bio-applications, highlighting its multifaceted role in various fields. Many heterocyclic derivatives were formed based on barbituric acid, for instance, pyrano-fused pyrimidine derivatives, spiro-oxindole derivatives, chrome-based barbituric acid derivatives, and many more via the atom economic method, Michael addition reaction, Knoevenagel condensation reaction, etc. In the context of bio-applications, this review examines the production of a wide range of bioactive drugs like anti-histamine, anti-leprotic, sedative–hypnotic, anti-inflammatory, anti-urease, antiviral, anti-AIDS, antimicrobial, antioxidant, anticonvulsant, anesthetic agent, antitumor, and anticancer drugs using efficient multicomponent reactions. By showcasing the versatility and potential of this compound, it aims to inspire further research and innovation in the field, leading to the development of novel barbituric acid derivatives with enhanced properties and diverse applications, with coverage of the literature relevant up to 2024.

The current study describes a novel and eco-conscious method to synthesize 1,4-dihydropyridine derivatives utilizing an aqueous micellar solution containing aluminum dodecyl sulfate, Al(DS)₃, using readily available starting material. The final products were synthesized with excellent yields within remarkably quick reaction durations, promoting remarkable atom economy and minimizing environmental impacts. The present protocol has several advantages over other methodologies in terms of high yield (up to 97%) with excellent purity. Further, the synthesized 1,4-DHPs exhibit favorable to excellent resistance against examined bacterial and fungal species. Intriguingly, polar groups on the phenyl ring (5b, 5c, 5i and 5j) make the 1,4-DHPs equally potent against the microbes as compared to the standard drugs.

The growth of the environment depends upon developing greener and ecological methods for managing pollutants and contamination from industrial wastewater, which causes significant effects on human health. The removal of these pollutants from wastewater using nanomaterials covers an ecological method that is free from expensive and secondary pollution. In this report, we developed magnetic iron nanoparticles from Chenopodium glaucum (CG), which showed excellent adsorption capacity at pH 5 for selective Hg²⁺ and Pb²⁺ metal ions among various heavy metal ions, with maximum adsorption capacities of 96.9 and 94.1%, respectively. These metals’ adsorption process conforms to the Langmuir model, which suggests that monolayer adsorption transpires on CG–Fe₂O₃ nanoparticles. CG–Fe₂O₃ nanoparticles also act as an efficient and recyclable heterogeneous catalyst for one-pot synthesis of xanthene derivatives, yielding products with high yields (up to 97%) and excellent purity (crystalline form) within a short timeframe (6 min) using microwave irradiations (at 120 W).

The magnetically recoverable heterogeneous Fe₂O₃@cellulose@Mn nanocomposite was synthesized by a stepwise fabrication of Mn nanoparticles on cellulose-modified magnetic Fe₂O₃ nanocomposites, and the morphology of the nanocomposite was characterized through advanced spectroscopic techniques. This nanocomposite was investigated as a heterogeneous catalyst for the synthesis of medicinally important tetrazole derivatives through Knoevenagel condensation between aromatic/heteroaromatic aldehyde and malononitrile followed by [3+2] cycloaddition reaction with sodium azide. Thirteen potent (E)-1-aryl-2-(1H-tetrazol-5-yl)acrylonitrile derivatives are reported in this paper with very high yields (up to 98%) and with excellent purity (as crystals) in a very short period (3 min @ 120 W) using microwave irradiation. The present procedure offers several advantages over recent protocols, including minimal catalyst loading, quick reaction time, and the utilization of an eco-friendly solvent. Furthermore, the synthesized (E)-1-aryl-2-(1H-tetrazol-5-yl)acrylonitrile derivatives (4b, 4c, and 4m) are shown to have excellent resistance against various fungal strains over bacterial strains as compared to the standard drugs Cefixime (4 μg/mL) and Fluconazole (2 μg/mL).

The discharge of dye-loaded textile effluents poses serious environmental concerns due to their high stability. In this study, a magnetic Fe₂O₃/TiO₂/NBC (FNT) heterostructure, derived from Cannabis sativa-based nanobiochar (NBC), was developed for crystal violet (CrV) degradation via peroxymonosulfate (PMS) activation. The crystalline structure, surface functional groups, morphology, and elemental composition were analyzed using advanced characterized of the synthesized catalyst. X-ray photoelectron spectroscopy (XPS) analysis confirmed the presence of Fe³⁺, Ti⁴⁺, and abundant surface oxygen species. Under UV light, efficient electron transfer across the FNT interface promoted PMS decomposition into hydroxyl and sulphate radicals. Electrochemical results indicated reduced charge recombination and enhanced electron mobility. Under optimal conditions (PMS = 75 mg/L, FNT = 30 mg/L, pH 7), 98.9% CrV degradation was achieved within 120 min. The catalyst maintained over 97% efficiency after five cycles, demonstrating excellent stability and reusability. Overall, this research demonstrates a robust and sustainable catalytic system for efficient dye degradation, offering strong potential for practical wastewater treatment applications.

Corrosion of mild steel (MS) in acidic environments presents a significant challenge in industrial applications, often leading to structural degradation and economic losses. This study investigated the effectiveness of Myrica esculenta (ME) extract as a green corrosion inhibitor for MS in acidic media. A combination of methods—including weight loss experiments, contact angle measurements, surface analysis, and electrochemical techniques—was employed to evaluate the inhibitor's performance. In the absence of the ME inhibitor, MS experienced rapid corrosion and significant weight loss. However, the addition of ME extract, particularly at a concentration of 40 mg/L, markedly reduced corrosion, achieving an inhibition efficiency of 86.93% after 12 hours. Electrochemical polarization studies revealed a shift in corrosion potential toward more noble values, indicating a reduced tendency for corrosion. Adsorption studies suggested that the inhibitor formed a protective layer through both monolayer and possible multilayer adsorption mechanisms. Contact angle analysis showed an increase in surface hydrophobicity, confirming the formation of a protective interface layer. UV analysis further validated the presence of this layer, which played a crucial role in minimizing pitting and preserving the structural integrity of the mild steel surface. These findings underscore the potential of ME as an effective and environmentally benign corrosion inhibitor.