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    	<title>IJPRS/V5/I4/00160 - 16/12/2016</title>

	<item>
		<title>Efficient Synthesis and Characterization of Novel 2-Aminobenzothiazole Derivatives</title>
		
		<description><![CDATA[<h5>Author's Affiliation</h5>
		                                                <p></p>
		                                                <hr/>
                                                    	<h5>Abstract</h5>
		                                                <p>Benzothiazole, a multifaceted nucleus, has been under research for the last two decades. Being a heterocyclic compound, benzothiazole finds use in research as a starting material for the synthesis of larger, usually bioactive structures. As a part of systematic investigations several new derivatives of 2-aminobenzothiazols 5a-e have been prepared. The structure elucidation of these compounds was completed by means of chemical tests, elemental (C, H, N and S) and spectral (IR,<sup> 1</sup>H NMR and mass) analysis.</p>
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                                                        <h5>Keywords</h5>
                                                         <p>2-aminobenzothiazole, benzamides, benzoyl isothiocyanate</p>
                                                         
                                                    	                                                    	<hr/>
                                                         <h5>Cite This Article</h5>
                                                         <p>Wanjari, P., Bharati, A., &amp; Ingle, V. (2016). Efficient Synthesis and Characterization of Novel 2-Aminobenzothiazole Derivatives, <em>International Journal for Pharmaceutical Research Scholars (IJPRS)</em>, 5(4), 108-112.</p>                                                         <hr/>
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		<link>https://www.ijprs.com/article/efficient-synthesis-and-characterization-of-novel-2-aminobenzothiazole-derivatives/</link>
		<author>Wanjari, P., Bharati, A., Ingle, V.        </author>

		<pdflink>http://www.ijprs.com/wp-content/uploads/2018/09/IJPRS-V5-I4-00160.pdf</pdflink>

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