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4-(tert-Butylamino)-3-[(ethoxycarbonyl)methyl]-1-methyl-2-(methylthio)-5-phenylimidazolium Chloride

Compound with spectra: 1 NMR, and 1 MS (GC)

4-(tert-Butylamino)-3-[(ethoxycarbonyl)methyl]-1-methyl-2-(methylthio)-5-phenylimidazolium Chloride
SpectraBase Compound ID 3MR0tr3ReQ0
InChI InChI=1S/C19H28N3O2S.ClH/c1-7-24-15(23)13-22-17(20-19(2,3)4)16(21(5)18(22)25-6)14-11-9-8-10-12-14;/h8-12,20H,7,13H2,1-6H3;1H/q+1;/p-1
InChIKey GPDHMRPOFRLTIG-UHFFFAOYSA-M
Mol Weight 397.97 g/mol
Molecular Formula C19H28ClN3O2S
Exact Mass 397.159076 g/mol
Parent InChIKey GWJGOVGETVNXJW-UHFFFAOYSA-M

View Spectrum of 4-(tert-Butylamino)-3-[(ethoxycarbonyl)methyl]-1-methyl-2-(methylthio)-5-phenylimidazolium Chloride

MS (GC) Spectrum
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Source of Spectrum J-57-2125-5

View Spectrum of 4-(tert-Butylamino)-3-[(ethoxycarbonyl)methyl]-1-methyl-2-(methylthio)-5-phenylimidazolium Chloride

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
3-Benzyl-4-(tert-butylamino)-1-methyl-2-(methylthio)-5-phenylimidazolium Chloride
1,3-DIISOPROPYL-2-(METHYLTHIO)-5-(4-NITROPHENYL)-4-(ISOPROPYLAMINO)-IMIDAZOLIUM-CHLORIDE
3-(3,4-dichlorophenyl)-1-[2-oxo-2-(4-phenoxyanilino)ethyl]-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-1-ium chloride
3-(4-chlorophenyl)-1-{2-[(2-isopropyl-5-methylcyclohexyl)oxy]-2-oxoethyl}-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-1-ium chloride
4-Phenyl-2,4-dihydro-5-((6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl)methyl)-3H-1,2,4-triazole-3-thione
N-tert-Butyl-6-(5-hydroxymethylfuran-2-yl)imidazo[2,1-b]thiazol-5-amine
3-[(1'-Methyl-4',5'-diphenylimidazol-2'-yl)thio]-2,2,4,4-tetramethyl-3-(methylthio)cyclobutanone
2-(2-Methyl-5-nitro-1-(2-phenoxyethyl)-1H-imidazol-4-yl)-benzaldehyde
N-{4-[5-(4-fluorophenyl)-2-methanesulfonyl-3-methyl-3H-imidazol-4-yl]pyridin-2-yl}acetamide
2-(4'-Bromophenyl)-3-(6'-phenylimidazo[2,1-b][thiazol-3'-yl)acetamido]-4-thiazolidinone
Title Journal or Book Year
Three-component cyclocondensations. An efficient synthesis of 4-amino-2-(methylthio)imidazolium salts via the reaction of methyl chlorothioimidates with benzaldimines and isocyanides. Autoxidation of the imidazole derivatives The Journal of Organic Chemistry 1992
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