Trisubstituted s-triazine hydrazones [N3C3(-OC6H4-p-CH=N-NH-C(O)-C6H4-p-X)3] (X = H, Br, Cl, F) were prepared in excellent yields by the reaction of p-substituted N’-(4-hydroxy-benzylidene)-hydrazides with cyanuric chloride. The structures were elucidated by elemental analysis, FT-IR, 1H, 13C NMR and MALDI-TOF mass spectrometry. These s-triazine hydrazone derivatives were evaluated for their in vitro antimicrobial and antimycobacterial activity using serial dilution method.
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