1-(2-Mesitylenesulfonyl)-3-nitro-1H-1,2,4-triazole

  • CAT Number: R000189
  • CAS Number: 74257-00-4
  • Molecular Formula: C11H12N4O4S
  • Molecular Weight: 296.301
  • Purity: ≥95%
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<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1-(2-Mesitylenesulfonyl)-3-nitro-1H-1,2,4-triazole (CAS&nbsp;74257-00-4) can be used as a c<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">ondensing reagent for oligonucleotide synthesis.</span></span></span>

Catalog Number R000189
CAS Number 74257-00-4
Molecular Formula

C11H12N4O4S

Purity 95%
Storage -20°C
IUPAC Name 3-nitro-1-(2,4,6-trimethylphenyl)sulfonyl-1,2,4-triazole
InChI InChI=1S/C11H12N4O4S/c1-7-4-8(2)10(9(3)5-7)20(18,19)14-6-12-11(13-14)15(16)17/h4-6H,1-3H3
InChIKey SFYDWLYPIXHPML-UHFFFAOYSA-N
SMILES CC1=CC(=C(C(=C1)C)S(=O)(=O)N2C=NC(=N2)[N+](=O)[O-])C
Reference

<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">O&#39;Flaherty, Derek K., and Christopher J. Wilds. &quot;Preparation of Intrastrand {G} O 6‐Alkylene‐O 6 {G} Cross‐Linked Oligonucleotides.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Current protocols in nucleic acid chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;66.1 (2016): 5-17.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Efimov, Ilya V. &quot;Recent methods for the synthesis of NH-1, 2, 3-triazoles (microreview).&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Chemistry of Heterocyclic Compounds</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;55.1 (2019): 28-30.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Chang, Yu-Cheng, Pei-Wen Chao, and Ching-Hsuan Tung. &quot;Sensitive luciferin derived probes for selective carboxypeptidase activity.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Bioorganic &amp; medicinal chemistry letters</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;21.13 (2011): 3931-3934.</span></span></span>

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