124497-59-2

Upstream product

• 70-11-1 α-bromoacetophenone 
• 4413-43-8 4-amino-5-(4-chloro-phenoxymethyl)-2,4-dihydro-[1,2,4]triazole-3-thione 
• 2381-75-1 (4-chlorophenoxy)acetic acid hydrazide 
• 686258-10-6 N-[(4-chloro-phenoxy)-acetyl]-hydrazinecarbodithioic acid 
• 106-48-9 4-chloro-phenol 
• 14426-42-7 ethyl p-chlorophenoxyacetate 

Relevant academic research and scientific papers

Synthesis and antibacterial activity of N-bridged heterocycles derived from aryloxymethyltriazoles

Reactions of 3-aryloxymethyl-4-amino-5-mercapto-1,2,4-triazoles 1 with aromatic carboxylic acids, furoic acid, oxalic acid, monochloroacetic acid and phenacyl bromide furnish various N-bridged heterocycles viz., triazolothiadiazoles, bistriazolothiadiazoles, triazolothiadiazinones and triazolothiadiazines. The structures of these N-bridged heterocycles are characterized on the basis of elemental analyses, IR, NMR and mass spectral data. Some of these compounds are also subjected to antibacterial screening studies.