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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 4605-14-5 Chemical Structure| 4605-14-5

Structure of Norspermine
CAS No.: 4605-14-5

Chemical Structure| 4605-14-5

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Product Details of [ 4605-14-5 ]

CAS No. :4605-14-5
Formula : C9H24N4
M.W : 188.31
SMILES Code : NCCCNCCCNCCCN
MDL No. :MFCD00008213

Safety of [ 4605-14-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 4605-14-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4605-14-5 ]

[ 4605-14-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 72652-32-5 ]
  • [ 4605-14-5 ]
  • N,N'-((propane-1'',3''-diylbis(azanediyl))bis(propane-3',1'-diyl))bis(4-bromo-1H-pyrrole-2-carboxamide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
30% With triethylamine; In tetrahydrofuran; at 20℃; for 18h;Inert atmosphere; General procedure: the coupling of substituted pyrroles with amine for synthesis of di-pyrroleanalogues 12-19.To a solution of pyrrole 2 (2 equiv.) in dry THF at r.t., under an atmosphere of nitrogen, amine(1 equiv.) and triethylamine (4 equiv.) were added dropwise. The mixture was stirred for 18-72 h and the solvent was removed in vacuo to give the crude product, which was purified as stated.
  • 2
  • [ 72652-32-5 ]
  • [ 4605-14-5 ]
  • N,N'-((propane-1'',3''-diylbis(azanediyl))bis(propane-3',1'-diyl))bis(4,5-dibromo-1H-pyrrole-2-carboxamide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
41% With triethylamine; In tetrahydrofuran; at 20℃; for 72h;Inert atmosphere; General procedure: the coupling of substituted pyrroles with amine for synthesis of di-pyrroleanalogues 12-19.To a solution of pyrrole 2 (2 equiv.) in dry THF at r.t., under an atmosphere of nitrogen, amine(1 equiv.) and triethylamine (4 equiv.) were added dropwise. The mixture was stirred for 18-72 h and the solvent was removed in vacuo to give the crude product, which was purified as stated.
 

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