1,4,8,11-Tetraazacyclotetradecane

For research use only. Not for therapeutic Use.

  • CAT Number: R039608
  • CAS Number: 295-37-4
  • Molecular Formula: C10H24N4
  • Molecular Weight: 200.33
  • Purity: ≥95%
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<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1,4,8,11-Tetraazacyclotetradecane (CAS&nbsp;295-37-4)&nbsp;is an azamacrocycle that forms more stable metal complexes as compared to open chain ligands. It&nbsp;can be used as a ligand in the synthesis of cyanide-bridged Fe<sup style="font-size: 10.8px; color: rgb(102, 94, 88); font-family: Arial, Helvetica, sans-serif;">III</sup>-Cu<sup style="font-size: 10.8px; color: rgb(102, 94, 88); font-family: Arial, Helvetica, sans-serif;">II</sup>&nbsp;complexes and&nbsp;Zn(II) complexes with flufenamic acid (flu).</span></span></span>


Catalog Number R039608
CAS Number 295-37-4
Synonyms

Cyclam; JM 1498; NSC 180811;

Molecular Formula C10H24N4
Purity ≥95%
Storage Store at +4C
IUPAC Name 1,4,8,11-tetrazacyclotetradecane
InChI InChI=1S/C10H24N4/c1-3-11-7-9-13-5-2-6-14-10-8-12-4-1/h11-14H,1-10H2
InChIKey MDAXKAUIABOHTD-UHFFFAOYSA-N
SMILES C1CNCCNCCCNCCNC1
Reference

<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.F&uuml;zerov&aacute;, Silvia, et al. &quot;Cyclam (1, 4, 8, 11-tetraazacyclotetradecane) with one methylphosphonate pendant arm: a new ligand for selective copper (II) binding.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Dalton transactions</i>&nbsp;17 (2005): 2908-2915.<br />
2.Shi, Jingwen, et al. &quot;A serials of sandwich-like trinuclear and one-dimensional chain cyanide-bridged iron (III)-copper (II) complexes: Syntheses, crystal structures and magnetic properties.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Journal of Solid State Chemistry</i>&nbsp;260 (2018): 59-66.<br />
3.Smolkov&aacute;, R., et al. &quot;Novel Zn (II) complexes with non-steroidal anti-inflammatory ligand, flufenamic acid: Characterization, topoisomerase I inhibition activity, DNA and HSA binding studies.&quot;&nbsp;<i style="font-family: Arial, sans-serif; font-size: 13px;">Journal of Inorganic Biochemistry</i>&nbsp;177 (2017): 143-158.</span></span></span>

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