I graduated from the College of science at the University of Baghdad with a bachelor's degree in 2003 and in 2004, I transitioned to the Ministry of Higher Education and Scientific Research, having ranked among the top ten students, and joined the Department of Pharmaceutical Chemistry as a pharmacist. I pursued a master's degree in college of science, which I completed in 2009, earning the title of Assistant Lecturer. I continued my academic journey
achelor's degree in 2003 and in 2004, I transitioned to the Ministry of Higher Education and Scientific Research, having ranked among the top ten students, and joined the Department of Pharmaceutical Chemistry as a pharmacist. I pursued a master's degree in college of science, which I completed in 2009, earning the title of Assistant Lecturer. I continued my academic jo
Technical responsible for the pharmaceutical chemistry lab, College of Pharmacy, University of Baghdad. Member
Technical responsible for the pharmaceutical chemistry lab, College of Pharmacy, University of Baghdad. Member of the examination committee Member, Pharmaceutical chemistry Department, College of Pharmacy, University of Baghdad
My research interests center on advancements in drug development, with a particular focus on innovative approaches in pharmaceutical chemistry education and the integration of modern technologies in drug discovery processes. I also explore the impact of chemical properties on drug efficacy and safety, aiming to contribute to both academic knowledge and practical applications in the field.
Pharmaceutical Analysis - Development and validation of analytical techniques for the quality control of drugs, including chromatography and spectroscopy.
Organic Chemistry analytical Chemistry
Supervision on undergraduate (5th class)
The present study deals with the synthesis of four different azo-azomethine derivatives; this is done by two steps; the first step is diazotization of sulfonamides (sulfanilamide, sulfacetamide, sulfamethoxazole, and sulfadiazine) separately, followed by the second step; the coupling reaction of diazotized compounds with isatin bis-Schiff base named 3-((4-nitrobenzylidene) hydrazono)indolin-2-one. The later one (bis-Schiff base) was synthesized by the reaction of 3-hydrazono-indolin-2-one with p-nitrobenzaldehyde. The chemical structures of newly synthesized compounds were approved on the basis of their FTIR, 1H-NMR, and CHNS elemental analysis data results. The synthesized azo compounds were tested in vitro for their antimicrobial potentia
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