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Pyridinium trifluoromethanesulfonate, min. 97%

Catalog Number
ACM52193541-2
Product Name
Pyridinium trifluoromethanesulfonate, min. 97%
Structure
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CAS
52193-54-1
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Synonyms
CTK1G8962; AKOS015852954; AC1MC242; FT-0700859; SCHEMBL318231; TR-018537; YWVYZMVYXAVAKS-UHFFFAOYSA-N; Pyridinium triflate; ACMC-209ky5;
IUPAC Name
pyridin-1-ium;trifluoromethanesulfonate;
Molecular Weight
229.173g/mol
Molecular Formula
C6H6F3NO3S;
Canonical SMILES
C1=CC=[NH+]C=C1.C(F)(F)(F)S(=O)(=O)[O-];
InChI
InChI=1S/C5H5N.CHF3O3S/c1-2-4-6-5-3-1;2-1(3,4)8(5,6)7/h1-5H;(H,5,6,7);
InChI Key
YWVYZMVYXAVAKS-UHFFFAOYSA-N;
Complexity
176
Covalently-Bonded Unit Count
2
Exact Mass
229.002g/mol
H-Bond Acceptor
6
H-Bond Donor
1
Heavy Atom Count
14
Monoisotopic Mass
229.002g/mol
Topological Polar Surface Area
79.7A^2
Application
Pyridinium trifluoromethanesulfonate, with a minimum purity of 97%, serves as a highly versatile catalyst in various chemical reactions. Its applications include the silylation of alcohols, especially when used in combination with silylbenzamide, enhancing its utility in synthetic processes. Additionally, it plays a critical role in facilitating the condensation reactions between alcohols and carboxylic acids, and in enabling the reaction of aromatic compounds with sulfonyl chlorides. It is also indispensable in the cracking of alkanes, the alkylation of alkenes, and the isomerization of alkanes, as well as trans-alkylation and trans-bromination of aromatics. Furthermore, it supports a range of Friedel-Crafts reactions, showcasing its broad applicability and importance in organic synthesis.
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