Head of Chemistry Department, College of Natural and Computation Sciences, Haramaya University, Ethiopia
Aschale, M., Head of Chemistry Department, College of Natural and Computation Sciences, Haramaya University, Ethiopia
The title compounds were prepared by the reaction of substituted primary amines with chloroacetylchloride in benzene. Structures of all these compounds have been elucidated by their elemental analysis, spectral studies and molecular weights. All the products were assayed for their antimicrobial activities against Staphylococcus aureus and Xanthomonas holcicola bacteria and Aspergillus niger and Fusarium oxysporum fungi and results were compared with that of reference drugs.
2 chloroacetanilide; 2 iodo 2 chloroacetanilide; 3 bromo 2 chloroacetanilide; 3 chloro 2 chloroacetanilide; 4 bromo 2 chloroacetanilide; 4 dimethylamino 2 chloroacetanilide; acetanilide derivative; amine; antifungal agent; antiinfective agent; benzene; carbendazim; chloramphenicol; chloride; unclassified drug; 2 chloroacetanilide; 3 bromo 2 chloroacetanilide; 3 chloro 2 chloroacetanilide; 4 bromo 2 chloroacetanilide; 4 dimethylamino 2 chloroacetanilide; acetanilide derivative; antibiotic agent; antifungal agent; carbendazim; chloramphenicol; iodo 2 chloroacetanilide; antibacterial activity; antifungal activity; article; Aspergillus niger; carbon nuclear magnetic resonance; controlled study; drug synthesis; Fusarium oxysporum; infrared spectroscopy; molecular weight; nonhuman; physical chemistry; proton nuclear magnetic resonance; Staphylococcus aureus; substitution reaction; ultraviolet spectroscopy; Xanthomonas; Xanthomonas holcicola; drug structure; drug synthesis; Xanthomonas holicicola