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OAJJUFDHOYOSSA-JHVJFLLYSA-N

Compound with spectra: 3 NMR

OAJJUFDHOYOSSA-JHVJFLLYSA-N
SpectraBase Compound ID LkjLBqzxXaP
InChI InChI=1S/C23H26N2O6/c1-15-9-10-20(23(2,3)17-7-5-4-6-8-17)21(11-15)31-22(26)16-12-18(24(27)28)14-19(13-16)25(29)30/h4-8,12-15,20-21H,9-11H2,1-3H3/t15-,20-,21-/m0/s1
InChIKey OAJJUFDHOYOSSA-JHVJFLLYSA-N
Mol Weight 426.47 g/mol
Molecular Formula C23H26N2O6
Exact Mass 426.179087 g/mol
Enantiomer InChIKey OAJJUFDHOYOSSA-IPHXSNPTSA-N

View Spectrum of OAJJUFDHOYOSSA-JHVJFLLYSA-N

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

View Spectrum of OAJJUFDHOYOSSA-JHVJFLLYSA-N

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

View Spectrum of OAJJUFDHOYOSSA-JHVJFLLYSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
2-(1-Methyl-1-phenyl-ethyl)-5-methyl-cyclohexyl 3,5-dinitro-benzoate
(1R,3R,4S)-8-Phenylmenthyl (1S,2S)-2-phenylcyclopropanecarboxylate
(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl-4,4,4-trifluoro-2-hydroxy-2-methylbutanoate
(-)-8-Phenylmenthyl 3-[2-(trimethylsilyl)ethenyl]cyclopropane-1-carboxylate
5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl 2-hydroxy-2,5,5-trimethyl-4-oxohexanoate
(1R,2S.5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (R)-.alpha.-Hydroxy-.alpha.-(4-iodophenyl)benzeneacetate
(2S,5S,1R)-5-METHYL-2-(1-METHYL-1-PHENYLETHYL)-CYCLOHEXYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-BUTANOATE;MAJOR-DIASTEREOMER
(2S,5S,1R)-5-METHYL-2-(1-METHYL-1-PHENYLETHYL)-CYCLOHEXYL-4,4,4-TRIFLUORO-3-(4-METHOXYANILINO)-BUTANOATE;MINOR-DIASTEREOMER
8'-(Phenylmenthyl) 3-hydroxy-4-phenylpropanoate
(+)-(E)-(1'R,2'S,5'R)-8'-PHENYLMENTHYL-6-CHLORO-5,5-DIFLUORO-6-(4-METHOXYPHENYLIMINO)-2-HEXANOATE
XQBRQPLBAKWFOB-MABODERHSA-N
Title Journal or Book Year
Chiral induction in photochemical reactions. Part 4. Conformational analysis and crystal structure of (–)-8-phenylmenthyl [(–)-(1R,2S,5R)-2-(1-methyl-1-phenylethyl)-5-methylcyclohexyl] phenylglyoxylates: their face-differentiating effect in photochemical oxetane formation J. Chem. Soc., Perkin Trans. 2 1988

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