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Merck

309281

Sigma-Aldrich

Iron(III) perchlorate hydrate

crystalline

Sinónimos:

Perchloric acid iron(III) salt hydrate

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About This Item

Fórmula lineal:
Fe(ClO4)3 · xH2O
Número de CAS:
Peso molecular:
354.20 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352000
PubChem Substance ID:
NACRES:
NA.22

form

crystalline

Quality Level

reaction suitability

reagent type: oxidant

impurities

<0.10% chloride

color

yellow

SMILES string

[Fe+3].[H]O[H].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O

InChI

1S/3ClHO4.Fe.H2O/c3*2-1(3,4)5;;/h3*(H,2,3,4,5);;1H2/q;;;+3;/p-3

Inchi Key

PFPIMAZLJXJVAN-UHFFFAOYSA-K

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Application

Catalyst for synthesis of:
  • Fullerene-fused lactones
  • α-Carbonyl furans via one-pot cyclization
  • Fullerodioxolanes via heterocyclization
  • Dialylated indoles via double alkylation
  • Aryl esters via oxidative esterification

Used as chemical actinometer based on photolysis of ferrioxalate in presence of polyoxometalate in aqueous solution

Oxidant for conducting polymer nanoparticles synthesized in ionic liquid by chemical polymerization
Iron(III) perchlorate hydrate is a useful starting material for the synthesis of a tris-salicylate Fe(III) complex having bidentate chelating units and in photolysis of ferrioxalate in presence of polyoxometalate in aqueous solution.

It can be used as a catalyst for synthesis of:
  • Fullerene-fused lactones
  • α-Carbonyl furans via one-pot cyclization
  • Fullerodioxolanes via heterocyclization
  • Fulleroxazolidines
  • Dialylated indoles via double alkylation
  • Aryl esters via oxidative esterification

Useful starting material for the synthesis of a tris-salicylate Fe(III) complex having bidentate chelating units which allow two coordination modes.

pictograms

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signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

5.1A - Strongly oxidizing hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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A facile access to [60] fullerene-fused 1, 3-dioxolanes: Reaction of [60] fullerene with aldehydes/ketones promoted by ferric perchlorate.
Li FB, et al
Organic Letters, 12(14), 3258-3261 (2010)
Diverse redox chemistry of photo/ferrioxalate system.
Wang Z, et al.
Royal Society of Chemistry Advances, 4(84), 44654-44658 (2014)
Ferric Perchlorate Promoted Reaction of [60] Fullerene with N-Sulfonyl Aldimines: Synthesis and Functionalization of Fulleroxazolidines.
Liu TX, et al.
The Journal of Organic Chemistry, 80(24), 11986-11992 (2015)
Iron salt-catalyzed cascade type one-pot double alkylation of indole with vinyl ketones.
Kobayashi JK, et al.
Tetrahedron, 66(22), 3917-3922 (2010)
Iron-Catalyzed Domino Process for the Synthesis of ?-Carbonyl Furan Derivatives via One-Pot Cyclization Reaction.
Jiang H
The Journal of Organic Chemistry, 75(15), 5347-5350 (2010)

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