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AKJOXJVUUXHZSA-UHFFFAOYSA-N

Compound with spectra: 2 NMR

AKJOXJVUUXHZSA-UHFFFAOYSA-N
SpectraBase Compound ID 7CFNNDsluzN
InChI InChI=1S/C12H19NO/c1-7(2)9-5-4-8(3)10-6-13-12(14)11(9)10/h8-11H,1,4-6H2,2-3H3,(H,13,14)
InChIKey AKJOXJVUUXHZSA-UHFFFAOYSA-N
Mol Weight 193.29 g/mol
Molecular Formula C12H19NO
Exact Mass 193.146664 g/mol

View Spectrum of AKJOXJVUUXHZSA-UHFFFAOYSA-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 AKJOXJVUUXHZSA-UHFFFAOYSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Bicyclo[2.2.2]oct-5-ene-1,2-dicarboxamide, N,N'-dipentyl-
ROJPNLMELFFFPY-FBXFSONDSA-N
2-NAPHTALENECARBOXALDEHYDE, 3,4,4a,5,6,7,8,8a-OCTAHYDRO-5-METHYL-8-(1-METHYLETHENYL)-
Methyl 2-[N-(tert-Butoxycarbonyl)aminomethyl]bicyclo[2.2.1]heptan-3-carboxylate
Benditerpe-2,6,15-Triene
Methyl [1'R,2'S,3'S,4'R]-2-(2'-formyl-4'-methyl-3'-(3"-oxobutyl)cyclohex-1'-yl]propenoate
2-NAPHTALENEMETHANOL, 3,4,4a,5,6,7,8,8a-OCTAHYDRO-5-METHYL-8-(1-METHYLETHENYL)-
CADINA-4,11-DIEN-14-OL
4,11(13)-CADINADIEN-12-AL
ARTEMISINIC_ALDEHYDE;AAA
Title Journal or Book Year
Transition metal catalyzed radical cyclization: new preparative route to .gamma.-lactams from allylic alcohols via the [3.3]-sigmatropic rearrangement of allylic trichloroacetimidates and the subsequent ruthenium-catalyzed cyclization of N-allyltrichloroacetamides The Journal of Organic Chemistry 1992

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