<?xml version="1.0"?>
<records>
  <record>
    <language>eng</language>
    <publisher>Ansari Education and Research Society</publisher>
    <journalTitle>Journal of Ultra Chemistry</journalTitle>
    <issn>0973-3450</issn>
    <eissn>2319-8036</eissn>
    <publicationDate>June 2006</publicationDate>
    <volume>2</volume>
    <issue>2</issue>
    <startPage>179</startPage>
    <endPage>182</endPage>
    <doi>juc</doi>
    <publisherRecordId>823</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis and antimicrobial activity of novel 3-(p-nitro phenoxy methyl)-4-(2,4,6-trinitro- phenyl)-5-aryl-1,2,4-triazole derivatives</title>
    <authors>
      <author>
        <name>Shobha Singh</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>A.K. Yadav</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Vandana Singh</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>D.K. Singh</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Daroga Singh</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Chemistry, T.D.P.G. College, Jaunpur (U.P.) INDIA</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p&gt;The condensation of 3-p-nitrophenoxy methyl acetate and hydrazine hydrate to give p-nitro-phenoxy acetyl hydrazide (1). The hydrazide (1) reacts with various aromatic acid in the presence of POCl3&amp;nbsp;to give 3-(p-nitro phenoxymethyl)-5-aryl-1,3,4-oxadiazole (3). Further these oxadiazole (3) condensed with 2,4,6-trinitroaniline to yield the title compounds (4). These compounds have been characterized by U.V., I.R. and PMR spectra. The antimicrobial activity of these compounds have also been screened.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/823/</fullTextUrl>
    <keywords>
      <keyword language="eng">antimicrobial activity</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">phenoxy methyl</keyword>
    </keywords>
  </record>
</records>
