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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2015-03-25</publicationDate>
    
        <volume>3</volume>
        <issue>1</issue>

 
    <startPage>141</startPage>
    <endPage>146</endPage>

	    <publisherRecordId>1254</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">An Efficient Synthesis, Characterization of some Novel 6 -(R) phenyl-azo-coumarin -3- carboxy(3-chloro- 4-methoxy) anilide and 2- hydroxy- 5(R)-phenyl &#8211; azo &#8211; benzylidine (3- chloro &#8211; 4 -methoxy)aniline and their Antibacterial Activity</title>

    <authors>
	 


      <author>
       <name>Alok K. Pareek</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>P. E. Joseph </name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Daya S. Seth</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">School of Chemical Sciences, Department of Chemistry, ST. John’s College, Agra - 282 002 India.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng"><p style="text-align: left;">An efficient synthesis of various substituted azo-coumarin &amp; azo-Schiff base has been synthesized by the condensation of 3-chloro-4-methoxy phenyl malon anilic acid (1a) and different substituted phenyl benzene-azo-salicylaldehyde (5a-5l) with few drops of pyridine as a condensing agent. The constitution of the newly synthesized products has been established on the basis of their spectral studies viz: IR, 1H NMR, Elemental analysis and physical properties as m.p, colour, yield%, molecular formula etc. and their antibacterial activity was carried out against S.aureus and E.coli micro-organisum.</p></abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol3no1/an-efficient-synthesis-characterization-of-some-novel-6-r-phenyl-azo-coumarin-3-carboxy3-chloro-4-methoxy-anilide-and-2-hydroxy-5r-phenyl-azo-benzylidine-3-chloro-4-methoxyanili/</fullTextUrl>

<keywords language="eng">

      
        <keyword><p style="text-align: left</keyword>
      

      
        <keyword>">Subs. Azo - Coumarins</keyword>
      

      
        <keyword> Azo - Schiff’s Bases</keyword>
      

      
        <keyword> Pyridine</keyword>
      

      
        <keyword> Condensation</keyword>
      

      
        <keyword> Malonic Acid</p></keyword>
      
</keywords>
  </record>
</records>