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<title><![CDATA[EC21 Product Catalogs - heterocyclic]]></title>
<link><![CDATA[https://www.ec21.com/ec-market/heterocyclic--0539/1/heterocyclic.html]]></link><item>
<title><![CDATA[N-Butyric Acid]]></title><link><![CDATA[https://global1za.en.ec21.com/N-Butyric-Acid--10878286_10878314.html]]></link><description><![CDATA[heterocycle and important intermediate of medici 
CLASS:8.3 
Relative density (25/25&amp;deg;C):0.956-0.959 
Refractive index:1.398-1.399 
Flashing point:70&amp;deg;C 
Heavy metal(Pb):&amp;le;0.001% 
Product Des]]></description><pubDate><![CDATA[20181220]]></pubDate></item>
<item>
<title><![CDATA[2-Octyl-2H-ISOTHIAZOL-3-one]]></title><link><![CDATA[https://20230420kmk.en.ec21.com/2-Octyl-2H-ISOTHIAZOL-3--11802628_11802711.html]]></link><description><![CDATA[Heterocyclic Compounds;Heterocycles;Intermediates &amp; Fine Chemicals;Pharmaceuticals
Melting point &lt;25 °C
Boiling point 120°C
density 1.04
vapor pressure 4.9hPa at 25℃
refractive index 1.5500 (esti]]></description><pubDate><![CDATA[20230606]]></pubDate></item>
<item>
<title><![CDATA[2-Imidazolidinone/ Ethylene Urea (CAS 120-93-4)]]></title><link><![CDATA[https://aogechem.en.ec21.com/2-Imidazolidinone-Ethylene-Urea--7647352_8274952.html]]></link><description><![CDATA[by a cyanoacetylation reaction for the synthesis of an antibacterial heterocycle; for the Pd-catalyzed reaction of a CN bond with a heteroaromatic tosylate; Of the oxidative amidation reaction
]]></description><pubDate><![CDATA[20171227]]></pubDate></item>

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