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515884

Sigma-Aldrich

Aluminum trifluoromethanesulfonate

99.9% trace metals basis

Synonym(s):

Aluminum tris(trifluoromethanesulfonate), Tris(trifluoromethanesulfonato)aluminum, Aluminum triflate

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About This Item

Linear Formula:
(CF3SO3)3Al
CAS Number:
74974-61-1
Molecular Weight:
474.19
MDL number:
MFCD00143596
UNSPSC Code:
12161600
PubChem Substance ID:
24873851
NACRES:
NA.22

Quality Level

100

Assay

99.9% trace metals basis

reaction suitability

core: aluminum
reagent type: catalyst

mp

300 °C (lit.)

SMILES string

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

InChI key

FKOASGGZYSYPBI-UHFFFAOYSA-K

Related Categories

Application

Aluminum trifluoromethanesulfonate (aluminum triflate or Al(OTf)3) can be employed as a catalyst:
  • In the regioselective synthesis of cyclic ethers by cycloisomerization of unsaturated alcohols.
  • In the conversion of saccharides into 5-hydroxymethylfurfural (5-HMF).
  • Along with Pd(OAc)2/BINAP for the methoxycarbonylation reaction of phenylacetylene.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

515884-VAR:
515884-BULK:
515884-50G:4548173943084
515884-10G:4548173943077

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM7228
MKCM6153
MKCG5652
MKCB1353V
MKBZ7259V

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Valorization of an underused sugar derived from hemicellulose: Efficient synthesis of 5-hydroxymethylfurfural from mannose with aluminum salt catalyst in dimethyl sulfoxide/water mixed solvent
Jia S, et al.
Royal Society of Chemistry Advances, 7(62), 39221-39227 (2017)
Aluminium (III) trifluoromethanesulfonate as an efficient catalyst for the intramolecular hydroalkoxylation of unactivated olefins: experimental and theoretical approaches
Coulombel L, et al.
Chemistry?A European Journal , 12(24), 6356-6365 (2006)
Recyclable Pd (OAc) 2/Ligand/Al (OTf) 3 Catalyst for the Homogeneous Methoxycarbonylation and Hydrocarboxylation Reactions of Phenylacetylene
Williams DBG, et al.
Organometallics, 30(18), 4968-4973 (2011)
Shaochen Zhang et al.
Science (New York, N.Y.), 364(6435), 45-51 (2019-04-06)
Accessing enantiomerically enriched amines often demands oxidation-state adjustments, protection and deprotection processes, and purification procedures that increase cost and waste, limiting applicability. When diastereomers can be formed, one isomer is attainable. Here, we show that nitriles, largely viewed as insufficiently
Gang Liu et al.
Chemical communications (Cambridge, England), 48(56), 7049-7051 (2012-06-12)
An unexpected silver triflate-catalyzed tandem reaction of N'-(2-alkynylbenzylidene)hydrazide with ketene through 6-endo-cyclization, [3+2] cycloaddition and rearrangement is reported. This reaction proceeds efficiently to generate the molecular complexity with the formation of four bonds in a one-pot procedure.
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