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#-32-(S)-MOSHER-AMIDE;(2'S,2''S)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC

Compound with spectra: 1 NMR

#-32-(S)-MOSHER-AMIDE;(2'S,2''S)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC
SpectraBase Compound ID LlZjvTMzunW
InChI InChI=1S/C31H39F3N2O8/c1-17-22(25(38)43-28(3,4)5)20(23(18(2)35-17)26(39)44-29(6,7)8)16-21(24(37)41-9)36-27(40)30(42-10,31(32,33)34)19-14-12-11-13-15-19/h11-15,21H,16H2,1-10H3,(H,36,40)/t21-,30-/m0/s1
InChIKey GWXNAYQAGVOIMU-JRPXNJEYSA-N
Mol Weight 624.7 g/mol
Molecular Formula C31H39F3N2O8
Exact Mass 624.265851 g/mol
Enantiomer InChIKey GWXNAYQAGVOIMU-IIMAJNMQSA-N

View Spectrum of #-32-(S)-MOSHER-AMIDE;(2'S,2''S)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#-32-(R)-MOSHER-AMIDE;(2'S,2''R)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC
4-[2,6-Dimethyl-3,5-bis(methoxycarbonyl)pyridin-4-yl]-2,2,5,5-tetramethyl-2,5-dihydropyrrol-1-yloxy radical
IMPURITY-III;3-ETHYL-5-METHYL-2-(2-AMINOETHOXYMETHYL)-4-(2-CHLOROPHENYL)-6-METHYL-3,5-PYRIDINEDICARBOXYLATE-SALT
2-Methyl-5-oxo-1-[1]benzopyrano[3,4-c]pyridinecarboxylic acid ethyl ester
(2'S)-2-(2'-AMINO-2'-METHOXYCARBONYL-ETHYL)-6-METHYL-4-PHENYL-PYRIDINE-3,5-DICARBOXYLIC-ACID-DI-TERT.-BUTYLESTER
4-Benzyl 2,3-diethyl 1-benzyl-5-methyl-1H-pyrrole-2,3,4-tricarboxylate
2-(2-phenyl-7,8-dihydrocyclohepta[b]pyrrol-1(6H)-yl)isoindoline-1,3-dione
Isradipine-A (-H2)
(S*,1'S*,4'R*)-(1-Methyl-2-methylene-4-phenethylcyclobutyl)-(6-nitrobenzo[d][1,3]dioxol-5-yl)methanol
Dimethyl 4,6-dimethyl-2-[2'-(trifluoromethyl)phenyl]pyridine-3,5-dicarboxylate
Title Journal or Book Year
Model Studies toward the Synthesis of Dihydropyrimidinyl and Pyridyl α-Amino Acids via Three-Component Biginelli and Hantzsch Cyclocondensations The Journal of Organic Chemistry 2003
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