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Iron(III) trifluoromethanesulfonate

greener alternative

90%

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Synonym(s):
Fe(CF3SO3)3, Ferric triflate, Ferric trifluoromethanesulfonate, Fe(CF3SO3)3, Fe(OTf)3, Iron 1,1,1-trifluoromethanesulfonic acid, Iron(III) triflate
Empirical Formula (Hill Notation):
C3F9FeO9S3
CAS Number:
Molecular Weight:
503.05
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

90%

form

powder

reaction suitability

core: iron
reagent type: catalyst

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

mp

183 °C

greener alternative category

SMILES string

[Fe+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F

InChI

1S/3CHF3O3S.Fe/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3

InChI key

OSHOQERNFGVVRH-UHFFFAOYSA-K

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This Item
290068513512698172
Zinc trifluoromethanesulfonate 98%

290068

Zinc trifluoromethanesulfonate

Iron(II) trifluoromethanesulfonate ≥85%

698172

Iron(II) trifluoromethanesulfonate

assay

90%

assay

98%

assay

≥99.7% trace metals basis

assay

≥85%

form

powder

form

-

form

-

form

powder

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

mp

183 °C

mp

≥300 °C (lit.)

mp

-

mp

>300 °C

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F

flash_point_c

> 110 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Hai-Jie Song et al.
ChemSusChem, 8(24), 4250-4255 (2015-11-28)
Using a metal triflate and Pd/C as catalysts, alkanes were prepared from bioderived furans in a one-pot hydrodeoxygenation (HDO) process. During the reaction, the metal triflate plays a crucial role in the ring-opening HDO of furan compounds. The entire reaction
Imtiyaz Ahmad Wani et al.
Organic & biomolecular chemistry, 16(16), 2910-2922 (2018-04-06)
Direct and expedient access to densely substituted tetrahydrocarbazoles and tetrahydrocycloheptadiindoles bearing multiple contiguous stereocentres has been achieved via a two-fold divergent diastereoselective (dr up to >99 : 1) transformation of 2-vinylindoles. The high-yielding conversions (yield up to 87%) that are amenable for
Yang Li et al.
Macromolecular bioscience, 20(11), e2000146-e2000146 (2020-06-23)
The conducting polymer polyethylenedioxythiophene doped with polystyrene sulfonate (PEDOT:PSS) has received great attention in the field of wearable bioelectronics due to its tunable high electrical conductivity, air stability, ease of processability, biocompatibility, and recently discovered self-healing ability. It has been
Raffaele Cucciniello et al.
ChemSusChem, 9(23), 3272-3275 (2016-11-24)
The present work deals with the production of monoalkyl glyceryl ethers (MAGEs) through a new reaction pathway based on the reaction of glycidol and alcohols catalyzed by Lewis acid-based catalysts. Glycidol is quantitatively converted with high selectivity (99 %) into MAGEs

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