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2-Mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride

Catalog Number
ACM862893810-1
Product Name
2-Mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride
Structure
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CAS
862893-81-0
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Synonyms
Bode Catalyst 3;862893-81-0;2-Mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride;SCHEMBL1079568;CTK8F4381;DTXSID10474970;MFCD09787523;2-(2,4,6-Trimethyl-phenyl)-2,5,6,7-tetrahydro-pyrrolo[2,1-c][1,2,4]triazol-4-yliumchloride;
IUPAC Name
2-(2,4,6-trimethylphenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-4-ium;chloride;
Molecular Weight
263.769g/mol
Molecular Formula
C14H18ClN3;
Canonical SMILES
CC1=CC(=C(C(=C1)C)N2C=[N+]3CCCC3=N2)C.[Cl-];
InChI
InChI=1S/C14H18N3.ClH/c1-10-7-11(2)14(12(3)8-10)17-9-16-6-4-5-13(16)15-17;/h7-9H,4-6H2,1-3H3;1H/q+1;/p-1;
InChI Key
KKBONGWVMVUYPA-UHFFFAOYSA-M;
Complexity
269
Covalently-Bonded Unit Count
2
Exact Mass
263.119g/mol
H-Bond Acceptor
2
Heavy Atom Count
18
Monoisotopic Mass
263.119g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
21.7A^2
Application
The purpose of 2-Mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride is to act as a versatile catalyst for a variety of chemical reactions. It is particularly effective in facilitating intermolecular hydroacylation of cyclopropenes, crossed acyloin condensations, and domino ring-opening redox amidation. Additionally, it plays a crucial role in Knoevenagel condensation, Claisen rearrangement, and Lewis acid- and N-heterocyclic carbene-catalyzed cyclocondensation reactions. Furthermore, it serves as a Bode catalyst for enantioselective cyclizations, demonstrating its broad applicability in advancing complex synthetic processes.
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