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(1-C-13,N-15)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE

Compound with spectra: 1 NMR

(1-C-13,N-15)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
SpectraBase Compound ID GS3K6qxNk6A
InChI InChI=1S/C13H25N3O2/c1-9(2)11-13(18-4)15-10(7-5-6-8-14)12(16-11)17-3/h9-11H,5-8,14H2,1-4H3/t10-,11+/m0/s1/i8+1,14+1
InChIKey ALCFKCQHEMKWLG-XJOHXHQASA-N
Mol Weight 257.35 g/mol
Molecular Formula C1213CH25N215NO2
Exact Mass 257.195067 g/mol
Enantiomer InChIKey ALCFKCQHEMKWLG-NDBBZWABSA-N

View Spectrum of (1-C-13,N-15)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2-C-13)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
(1-C-13)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
(2-C-13)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
(1-C-13)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYLAMINE
(1-C-13,N-15)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYRONITRILE
(1-C-13)-4-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-BUTYRONITRILE
3-[(2R,5S)-2,5-DIHYDRO-2-ISOPROPYL-3,6-DIMETHOXY-5-PYRAZINYL]-PROPYL-BROMIDE
(2R,5S)-2,5-Dihydro-3,6-dimethoxy-2-isopropyl-5-(4-pentenyl)pyrazine
(2R)-2-(3-Butenyl)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazine
(2R,5S)-2-but-3-enyl-3,6-dimethoxy-5-propan-2-yl-2,5-dihydropyrazine
(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-propa-1,2-dienyl-2,5-dihydro-pyrazine
(3S,6R)-6-(2'-CHLOROMETHYLPROP-2'-ENYL)-3-PROPYL-2,5-DIMETHOXY-3,6-DIHYDROPYRAZINE
(4S,2'R)-2-((3,3-dimethyl-2-methylenecyclohex-1-yl)methyl)-4,5-dihydro-4-(1-methylethyl)oxazole
Title Journal or Book Year
Enantioselective syntheses of isotopically labelled α-amino acids. Preparation of (ϵ-13C)-L-α-aminoadipic acid and five isotopomers of L-lysine with 13C, 15N and 2H in the δ- and ϵ-positions Recueil des Travaux Chimiques des Pays-Bas 2010
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