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2-Mesityl-5-methylimidazo[1,5-a]pyridinium chloride

Catalog Number
ACM1034449187
Product Name
2-Mesityl-5-methylimidazo[1,5-a]pyridinium chloride
CAS
1034449-18-7
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Synonyms
1034449-18-7;2-Mesityl-5-methylimidazo[1,5-a]pyridinium chloride;SCHEMBL819011;CTK8F4382;DTXSID00584911;2-(2,4,6-Trimethylphenyl)-5-methylimidazo[1,5-a]pyridinim chloride;2-Mesityl-5-methylimidazo[1,5-a]pyridinium chloride, 97%;5-Methyl-2-(2,4,6-trimethylphenyl)-2H-imidazo[1,5-a]pyridin-4-ium chloride;
IUPAC Name
5-methyl-2-(2,4,6-trimethylphenyl)imidazo[1,5-a]pyridin-2-ium;chloride;
Molecular Weight
286.803g/mol
Molecular Formula
C17H19ClN2;
Canonical SMILES
CC1=CC=CC2=C[N+](=CN12)C3=C(C=C(C=C3C)C)C.[Cl-];
InChI
InChI=1S/C17H19N2.ClH/c1-12-8-13(2)17(14(3)9-12)18-10-16-7-5-6-15(4)19(16)11-18;/h5-11H,1-4H3;1H/q+1;/p-1;
InChI Key
DJFXURXZOPNPGY-UHFFFAOYSA-M;
Complexity
304
Covalently-Bonded Unit Count
2
Exact Mass
286.124g/mol
H-Bond Acceptor
1
Heavy Atom Count
20
Monoisotopic Mass
286.124g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
8.3A^2
Application
The purpose of 2-Mesityl-5-methylimidazo[1,5-a]pyridinium chloride is to serve as a reactant in gold-catalyzed cycloisomerization reactions. This compound plays a crucial role in facilitating these catalytic processes, enabling the transformation of various substrates into cyclized products efficiently. Its specialized structure contributes to the overall effectiveness of the reaction, making it an invaluable component in the synthesis of complex organic molecules.
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