s-Triazines (3) were synthesized by the reaction of formaldehyde with substituted benzoic hydrazides (2). Structural assignments of newly synthesized compounds are based on the analytical and spectral data.The final compound(3) were screened against various bacteria viz staphylococcus aurous(Sa) Enterococcus facalis(Ef) and Escherichia Coli(Ec) involving two strains of (Sa) and (Ef) and only one of (Ec) as recommended by NCCLS, Moxifloxacin and linezolid were taken as reference standard.
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