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	<title>Building Blocks &#8211; ChemiMart</title>
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	<link>https://www.chemimart.de</link>
	<description>Professional expertise in chemical research and preparation of complex organic compounds from Berlin-Adlershof. We do chemistry for you!</description>
	<lastBuildDate>Thu, 08 Dec 2022 15:44:28 +0000</lastBuildDate>
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	<title>Building Blocks &#8211; ChemiMart</title>
	<link>https://www.chemimart.de</link>
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	<item>
		<title>2-​((2-​Aminoethylthio)​methyl)​-​5-​((N,​N-​dimethylamino)​methyl)​furan</title>
		<link>https://www.chemimart.de/product/2-%e2%80%8b2-%e2%80%8baminoethylthio%e2%80%8bmethyl%e2%80%8b-%e2%80%8b5-%e2%80%8bn%e2%80%8bn-%e2%80%8bdimethylamino%e2%80%8bmethyl%e2%80%8bfuran/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:33:01 +0000</pubDate>
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					<description><![CDATA[Ranitidine USP RC A ; Ranitidine Aminoethyl Impurity; Ranitidine impurity-​B (BP​/EP).]]></description>
										<content:encoded><![CDATA[<p>Ranitidine USP RC A ; Ranitidine Aminoethyl Impurity; Ranitidine impurity-​B (BP​/EP).</p>
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		<item>
		<title>Hydroquinone bis(10-undecenyl) ether</title>
		<link>https://www.chemimart.de/product/hydroquinone-bis10-undecenyl-ether/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:30:31 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=458</guid>

					<description><![CDATA[This structure finds application in liquid-crystal elastomers and materials science. Ref.: 1) Synthesis and Crystallization Behavior of Equisequential ADMET Polyethylene Containing Arylene Ether Defects: Remarkable Effects of Substitution Position and Arylene Size S.-F. Song, Y.-T. Guo, R.-Y. Wang, Z.-S. Fu, J.-T. Xu, Z.-Q. Fan Macromolecules, 2016, 49, 6001-6011 DOI: 10.1021/acs.macromol.6b01324]]></description>
										<content:encoded><![CDATA[<p>This structure finds application in liquid-crystal elastomers and materials science.</p>
<p><em>Ref.:</em></p>
<p>1) Synthesis and Crystallization Behavior of Equisequential ADMET Polyethylene Containing Arylene Ether Defects: Remarkable Effects of Substitution Position and Arylene Size</p>
<p>S.-F. Song, Y.-T. Guo, R.-Y. Wang, Z.-S. Fu, J.-T. Xu, Z.-Q. Fan <em>Macromolecules, </em><strong>2016</strong>, <em>49</em>, 6001-6011</p>
<p>DOI: 10.1021/acs.macromol.6b01324</p>
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		<item>
		<title>Ethyl 2-((tert-butoxycarbonyl)amino)-3,3,3-trifluoro-2-hydroxypropanoate</title>
		<link>https://www.chemimart.de/product/ethyl-2-tert-butoxycarbonylamino-333-trifluoro-2-hydroxypropanoate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:26:55 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=453</guid>

					<description><![CDATA[This derivative can be used to synthesize CF3-bearing quaternary amino acids. Ref.: &#160; 1)  Synthesis of α-​(trifluoromethyl)​-​substituted α-​amino acids. 8. New synthetic pathways to 3,​3,​3-​trifluoroalanine, 2-​deutero-​3,​3,​3-​trifluoroalanine and their derivatives Burger, Klaus; Hoess, Eva; Gaa, Karl; Sewald, Norbert; Schierlinger, Christian Zeitschrift fuer Naturforschung, B:  Chemical Sciences, 1991, 46, 361-384 DOI: 10.1515/znb-1991-0316]]></description>
										<content:encoded><![CDATA[<p>This derivative can be used to synthesize CF3-bearing quaternary amino acids.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Synthesis of α-​(trifluoromethyl)​-​substituted α-​amino acids. 8. New synthetic pathways to 3,​3,​3-​trifluoroalanine, 2-​deutero-​3,​3,​3-​trifluoroalanine and their derivatives</p>
<p>Burger, Klaus; Hoess, Eva; Gaa, Karl; Sewald, Norbert; Schierlinger, Christian<br />
<em>Zeitschrift fuer Naturforschung, B:  Chemical Sciences</em>, <strong>1991</strong>, <em>46</em>, 361-384<br />
DOI: 10.1515/znb-1991-0316</p>
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			</item>
		<item>
		<title>Ethyl (E)-2-((tert-butoxycarbonyl)imino)-3,3,3-trifluoropropanoate</title>
		<link>https://www.chemimart.de/product/ethyl-e-2-tert-butoxycarbonylimino-333-trifluoropropanoate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:24:58 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=448</guid>

					<description><![CDATA[Trifluoropyruvate ketimine derivative that can be used to synthesize CF3-bearing quaternary amino acids. Ref.: &#160; 1)  Enantioselective Organocatalytic Synthesis of Quaternary α-Amino Acids Bearing a CF3 Moiety Ralph Husmann, Erli Sugiono, Stefanie Mersmann, Gerhard Raabe, Magnus Rueping, and Carsten Bolm Organic Letters, 2011, 13, 1044-1047 DOI: 10.1021/ol103093r]]></description>
										<content:encoded><![CDATA[<p>Trifluoropyruvate ketimine derivative that can be used to synthesize CF3-bearing quaternary amino acids.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Enantioselective Organocatalytic Synthesis of Quaternary α-Amino Acids Bearing a CF3 Moiety</p>
<p>Ralph Husmann, Erli Sugiono, Stefanie Mersmann, Gerhard Raabe, Magnus Rueping, and Carsten Bolm<br />
<em>Organic Letters</em>, <strong>2011</strong>, <em>13</em>, 1044-1047<br />
DOI: 10.1021/ol103093r</p>
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			</item>
		<item>
		<title>4-Methoxyphenyl 4-(3-butenyloxy)benzoate</title>
		<link>https://www.chemimart.de/product/4-methoxyphenyl-4-3-butenyloxybenzoate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:22:52 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=445</guid>

					<description><![CDATA[Ref.: 1) Near-Infrared Responsive Liquid Crystalline Elastomers Containing Photothermal Conjugated Polymers W. Liu, L.-X. Guo, B.-P. Lin, X.-Q. Zhang, Y. Sun, H. Yang Macromolecules, 2016, 49, 4023-4030 DOI: 10.1021/acs.macromol.6b00640]]></description>
										<content:encoded><![CDATA[<p><em>Ref.:</em></p>
<p>1) Near-Infrared Responsive Liquid Crystalline Elastomers Containing Photothermal Conjugated Polymers</p>
<p>W. Liu, L.-X. Guo, B.-P. Lin, X.-Q. Zhang, Y. Sun, H. Yang<em> Macromolecules, </em><strong>2016</strong><em>, 49, </em>4023-4030</p>
<p>DOI: 10.1021/acs.macromol.6b00640</p>
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			</item>
		<item>
		<title>3,6-Dichlorotrimellitic acid</title>
		<link>https://www.chemimart.de/product/36-dichlorotrimellitic-acid/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:20:58 +0000</pubDate>
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					<description><![CDATA[3,6-Dichlorotrimellitic acid is the key precursor for preparing a variety of dichlorinated fluoresceins/rhodamines. Ref.: 1) Improved Synthetic Procedures for 4,7,2&#8242;,7&#8242;-Tetrachloro- and 4&#8242;,5&#8242;-Dichloro-2&#8242;,7&#8242;-dimethoxy-5(and 6)-carboxyfluoresceins M. H. Lyttle, T. G. Carter, R. M. Cook Organic Process Research &#38; Development, 2001, 5, 45-49 DOI: 10.1021/op000292o]]></description>
										<content:encoded><![CDATA[<p>3,6-Dichlorotrimellitic acid is the key precursor for preparing a variety of dichlorinated fluoresceins/rhodamines.</p>
<p><em>Ref.:</em></p>
<p>1) Improved Synthetic Procedures for 4,7,2&#8242;,7&#8242;-Tetrachloro- and 4&#8242;,5&#8242;-Dichloro-2&#8242;,7&#8242;-dimethoxy-5(and 6)-carboxyfluoresceins</p>
<p>M. H. Lyttle, T. G. Carter, R. M. Cook <em>Organic Process Research &amp; Development</em>, <strong>2001</strong>, <em>5</em>, 45-49</p>
<p>DOI: 10.1021/op000292o</p>
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			</item>
		<item>
		<title>3,5-Dichloro-2,4-dihydroxybenzoic acid</title>
		<link>https://www.chemimart.de/product/35-dichloro-24-dihydroxybenzoic-acid/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:18:52 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=438</guid>

					<description><![CDATA[Key precursor for preparing a variety of fluoresceins/rhodamines. Ref.: 1) Octachloro-fluorescein: Synthesis and photosensitizer performance evaluation Y. Wang, H. Chen, C. Li, P. Wu Dyes and Pigments, 2019, 170, 107635 DOI: 10.1016/j.dyepig.2019.107635]]></description>
										<content:encoded><![CDATA[<p>Key precursor for preparing a variety of fluoresceins/rhodamines.</p>
<p><em>Ref.:</em></p>
<p>1) Octachloro-fluorescein: Synthesis and photosensitizer performance evaluation</p>
<p>Y. Wang, H. Chen, C. Li, P. Wu <em>Dyes and Pigments, </em><strong>2019, </strong><em>170, </em>107635</p>
<div>DOI: 10.1016/j.dyepig.2019.107635</div>
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			</item>
		<item>
		<title>2,4-Dichlororesorcinol</title>
		<link>https://www.chemimart.de/product/24-dichlororesorcinol/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:17:11 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=434</guid>

					<description><![CDATA[Key precursor for preparing a variety of fluoresceins/rhodamines. Ref.: 1) Octachloro-fluorescein: Synthesis and photosensitizer performance evaluation Y. Wang, H. Chen, C. Li, P. Wu Dyes and Pigments, 2019, 170, 107635 DOI: 10.1016/j.dyepig.2019.107635]]></description>
										<content:encoded><![CDATA[<p>Key precursor for preparing a variety of fluoresceins/rhodamines.</p>
<p><em>Ref.:</em></p>
<p>1) Octachloro-fluorescein: Synthesis and photosensitizer performance evaluation</p>
<p>Y. Wang, H. Chen, C. Li, P. Wu <em>Dyes and Pigments, </em><strong>2019, </strong><em>170, </em>107635</p>
<div>DOI: 10.1016/j.dyepig.2019.107635</div>
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			</item>
		<item>
		<title>2-((triisopropylsilyl)ethynyl)propane-1,2,3-triol</title>
		<link>https://www.chemimart.de/product/2-triisopropylsilylethynylpropane-123-triol/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:15:23 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=430</guid>

					<description><![CDATA[C-3 glycerol derivative. Ref.: &#160; 1)  Enantioselective Synthesis of 4′-Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA) via Enzymatic Desymmetrization M. McLaughlin, J. Kong, K. M. Belyk, B. Chen, A. W. Gibson, S. P. Keen, D. R. Lieberman, E. M. Milczek, J. C. Moore, D. Murray, F. Peng, J. Qi, R. A. Reamer, Z. J. Song, L. Tan, L. Wang, M. J. [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>C-3 glycerol derivative.</p>
<p><em><br />
Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Enantioselective Synthesis of 4′-Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA) via Enzymatic Desymmetrization</p>
<p>M. McLaughlin, J. Kong, K. M. Belyk, B. Chen, A. W. Gibson, S. P. Keen, D. R. Lieberman, E. M. Milczek, J. C. Moore, D. Murray, F. Peng, J. Qi, R. A. Reamer, Z. J. Song, L. Tan, L. Wang, M. J. Williams <em>Organic Letters</em>, <strong>2017</strong>, <em>19</em>, 926-929<br />
DOI: 10.1021/acs.orglett.7b00091</p>
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			</item>
		<item>
		<title>(R)-2-hydroxy-2-(hydroxymethyl)-4-(triisopropylsilyl)but-3-yn-1-yl acetate</title>
		<link>https://www.chemimart.de/product/r-2-hydroxy-2-hydroxymethyl-4-triisopropylsilylbut-3-yn-1-yl-acetate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:13:47 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=426</guid>

					<description><![CDATA[Chiral glycerol derivative ideal for furanose synthesis. Ref.: &#160; 1)  Enantioselective Synthesis of 4′-Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA) via Enzymatic Desymmetrization M. McLaughlin, J. Kong, K. M. Belyk, B. Chen, A. W. Gibson, S. P. Keen, D. R. Lieberman, E. M. Milczek, J. C. Moore, D. Murray, F. Peng, J. Qi, R. A. Reamer, Z. J. Song, L. Tan, [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Chiral glycerol derivative ideal for furanose synthesis.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Enantioselective Synthesis of 4′-Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA) via Enzymatic Desymmetrization</p>
<p>M. McLaughlin, J. Kong, K. M. Belyk, B. Chen, A. W. Gibson, S. P. Keen, D. R. Lieberman, E. M. Milczek, J. C. Moore, D. Murray, F. Peng, J. Qi, R. A. Reamer, Z. J. Song, L. Tan, L. Wang, M. J. Williams <em>Organic Letters</em>, <strong>2017</strong>, <em>19</em>, 926-929<br />
DOI: 10.1021/acs.orglett.7b00091</p>
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