Department Of Chemistry

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Browsing Department Of Chemistry by Subject "2-aminothiophenol"

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  • Item
    Open Access
    Synthesis and Antimicrobial Activity of Schiff Bases derived from substituted Salicyladehyde with 2-aminophenol and 2-aminothiophenol
    (Journal of Scientific Research and Development, 2013-01) Fasina, T.M.; Ejiah, F.N.; Dueke-Eze, C.U.; Idika, N.
    Schiff bases of substituted salicylaldehydes namely 5-bromosalicylaldehyde and 5-nitrosalicyladehyde with 2- aminophenol and 2-aminothiophenol have been synthesized and characterized by IR, NMR and elemental analysis. All synthesized compounds were screened for their antimicrobial activity against some clinically important bacteria; Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Staphylococcus aureus ATCC25923, Enterococcus feacalis ATCC 29212 by Agar ditch method using N,N’-dimethylformamide (DMF) and 1,4-dioxane as solvents. Activity data shows a higher activity of the compounds in DMF with the bromo substituted imines more potent than the nitro substituted compounds
  • Item
    Open Access
    Synthesis and Antimicrobial Activity of Schiff Bases derived from substituted Salicyladehyde with 2-aminophenol and 2-aminothiophenol
    (Journal of Scientific Research and Development, 2013-01) Fashina, T.M.; Ejiah, F.N.; Dueke-Eze, C.U.; Idika, N.
    Schiff bases of substituted salicylaldehydes namely 5-bromosalicylaldehyde and 5-nitrosalicyladehyde with 2- aminophenol and 2-aminothiophenol have been synthesized and characterized by IR, NMR and elemental analysis. All synthesized compounds were screened for their antimicrobial activity against some clinically important bacteria; Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Staphylococcus aureus ATCC25923, Enterococcus feacalis ATCC 29212 by Agar ditch method using N,N’-dimethylformamide (DMF) and 1,4-dioxane as solvents. Activity data shows a higher activity of the compounds in DMF with the bromo substituted imines more potent than the nitro substituted compound