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N1-[2'-(4''-CHLORO)-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL

Compound with spectra: 2 NMR

N1-[2'-(4''-CHLORO)-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL
SpectraBase Compound ID KbwTqCHLZQ8
InChI InChI=1S/C18H21ClN4O4/c1-10(24)13(11-6-8-12(19)9-7-11)14(25)23-16(27)22(5)18(3)17(23,2)20-15(26)21(18)4/h6-9,13H,1-5H3,(H,20,26)/t13?,17-,18+/m1/s1
InChIKey WNLZNUKRMCEZKU-YMSDKTMASA-N
Mol Weight 392.84 g/mol
Molecular Formula C18H21ClN4O4
Exact Mass 392.125133 g/mol
Enantiomer InChIKey WNLZNUKRMCEZKU-UGGKNOJYSA-N

View Spectrum of N1-[2'-(4''-CHLORO)-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of N1-[2'-(4''-CHLORO)-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
N1-[2'-(4''-METHOXY)-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL
N1(2'-PHENYL-3'-OXO-BUTANOYL]-3,4,7,8-TETRAMETHYLGLYCOLURIL
11,14-Dihydroxy-2,3-epoxy-mutilan
BENZOXAZOMYCIN
#7I;(1-ALPHA,4-ALPHA,4A-ALPHA,7A-ALPHA)-4,4A,7,7A-TETRAHYDRO-8,8-DIMETHYL-1-(4'-METHOXYPHENYL)-4-(4''-NITROPHENYL)-1,4-METHANO-1H-CYCLOPENTA-[D]-PYRIDAZINE
#7J;(1-ALPHA,4-ALPHA,4A-ALPHA,7A-ALPHA)-4,4A,7,7A-TETRAHYDRO-8,8-DIMETHYL-1-(4'-METHYLPHENYL)-4-(4''-CARBOMETHOXYPHENYL)-1,4-METHANO-1H-CYCLOPENTA-[D]-PYRIDAZIN
(6S,7R)-6-(3-chlorophenyl)-8-methyl-3,4,6,7-tetrahydro-2H-1,4-benzothiazine-5,7-dicarboxylic acid O5-ethyl ester O7-methyl ester
Acetic acid, 3,4-diacetoxy-8-(2-acetoxy-2-cyanoethyl)-1,4a-dimethyl-7-oxotetradecahydrophenanthren-2-yl ester
1-{2,2-Di-tert-butyl-5-[(2,2-di-tert-butyl-4-oxo-4H-1,3,2-dioxasilin-6-yl)methyl]naphtho[1,8-de][1,3,2]dioxasilin-4-yl}-3-hydroxyhex-2-ene-1,5-dione
(2S,2'R)-3.beta.-Methoxy-2-[2'-Hydroxyperoxy-3'-(phenylsulfonyl)propyl]-5.alpha.-cholestan-3-one 2',3-peroxyhemiacetal
Title Journal or Book Year
Regioselectivity of glycoluril-directed Claisen condensations — A kinetic and mechanistic study of substituent effects in the nucleophilic acyl group Canadian Journal of Chemistry 2006
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