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	<dc:title xml:lang="en-US">Synthesis and antimicrobial activity of 1,3-bis-butyl-5-(4-iodophenyl)-1,3,5-triazacyclohexane</dc:title>
	<dc:creator>Lefrada, Leila</dc:creator>
	<dc:creator>Köhn, Randolf</dc:creator>
	<dc:creator>Malki, Souhila</dc:creator>
	<dc:creator>Mazouz, Wissam</dc:creator>
	<dc:creator>Bouchemma, Ahcene</dc:creator>
	<dc:creator>Hadjem, Meriem</dc:creator>
	<dc:subject xml:lang="en-US">Formalin</dc:subject>
	<dc:subject xml:lang="en-US">Synthesis</dc:subject>
	<dc:subject xml:lang="en-US">n-Butylamine</dc:subject>
	<dc:subject xml:lang="en-US">4-Iodoaniline</dc:subject>
	<dc:subject xml:lang="en-US">Triazacyclohexane</dc:subject>
	<dc:subject xml:lang="en-US">Antibacterial activity</dc:subject>
	<dc:description xml:lang="en-US">This work describes the synthesis, structural characterization and antibacterial activities of 1,3,5-triazacyclohexane type of new compound 1,3-bis-butyl-5-(4-iodophenyl)-1,3,5-triazacyclohexane. The new triazacyclohexanes (R3TAC) with mixed aryl and alkyl N-substituents are synthesized by the reaction of a 1:2 mixture of 4-iodoaniline and n-butylamine with formalin. The synthesized compounds were characterized by spectral analysis IR, 1H NMR and 13C NMR. The compound was screened for it’s antibacterial activity against Gram-positive and Gram-negative bacteria by the diffusion method on agar medium.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2017-03-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1537</dc:identifier>
	<dc:identifier>10.5155/eurjchem.8.1.82-84.1537</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 8 No. 1 (2017): March 2017; 82-84</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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