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IRON(III) PERCHLORATE HYDRATE

Base Information Edit
  • Chemical Name:IRON(III) PERCHLORATE HYDRATE
  • CAS No.:13537-24-1
  • Molecular Formula:ClH O4 . 1/3 Fe
  • Molecular Weight:372.21
  • Hs Code.:
  • Mol file:13537-24-1.mol
IRON(III) PERCHLORATE HYDRATE

Synonyms:Ironperchlorate (Fe(ClO4)3) (6CI,7CI); Perchloric acid, iron(3+) salt (8CI,9CI);Ferric perchlorate; Ferric perchlorate (Fe(ClO4)3); Iron triperchlorate;Iron(3+) perchlorate; Iron(III) perchlorate

Suppliers and Price of IRON(III) PERCHLORATE HYDRATE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Iron(III) perchlorate hydrate crystalline, low chloride
  • 500 g
  • $ 206.00
  • Sigma-Aldrich
  • Iron(III) perchlorate hydrate crystalline, low chloride
  • 100 g
  • $ 66.10
  • Sigma-Aldrich
  • Iron(III) perchlorate hydrate crystalline
  • 100 g
  • $ 53.30
Total 12 raw suppliers
Chemical Property of IRON(III) PERCHLORATE HYDRATE Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:222.81000 
  • Density:g/cm3 
  • LogP:0.64040 
  • Sensitive.:Hygroscopic 
Purity/Quality:

99% *data from raw suppliers

Iron(III) perchlorate hydrate crystalline, low chloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:O,Xi 
  • Statements: 8-36/37/38 
  • Safety Statements: 17-26-27 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
Refernces Edit

A novel three-component reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines

10.1016/j.tetlet.2008.11.123

The research focuses on the development of a novel three-component reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines, which are nitrogen-containing heterocyclic compounds with significant biological activity and applications in drug discovery and various chemical industries. The study utilizes a three-component condensation reaction catalyzed by ferric perchlorate, involving o-phenylenediamine, aromatic aldehydes, and cyclohexyl isocyanide, to produce the desired quinoxaline derivatives in good yields. The experiments were conducted by refluxing a mixture of the three reactants in acetonitrile with a catalytic amount of ferric perchlorate for 2 hours. The progress of the reactions was monitored by thin-layer chromatography (TLC), and the products were obtained without further purification after the reaction mixture was diluted, separated, and dried. The synthesized compounds were characterized using melting point determination, infrared spectroscopy (IR), proton and carbon nuclear magnetic resonance (1H NMR and 13C NMR), gas chromatography-mass spectrometry (GC/MS), and elemental analysis, which confirmed their structures and composition.

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