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TRIMETHYL-[(+/-)-1-BETA-TERT.-BUTOXY-7A-BETA-METHYL-2,3,3A-ALPHA,6,7,7A-HEXAHYDRO-5(4H)-OXO]-1H-INDEN-6-ALPHA-YL-METHYL-AMMONIUMIODIDE

Compound with spectra: 1 NMR

TRIMETHYL-[(+/-)-1-BETA-TERT.-BUTOXY-7A-BETA-METHYL-2,3,3A-ALPHA,6,7,7A-HEXAHYDRO-5(4H)-OXO]-1H-INDEN-6-ALPHA-YL-METHYL-AMMONIUMIODIDE
SpectraBase Compound ID EkPJTVS3v7o
InChI InChI=1S/C18H34NO2.HI/c1-17(2,3)21-16-9-8-14-10-15(20)13(11-18(14,16)4)12-19(5,6)7;/h13-14,16H,8-12H2,1-7H3;1H/q+1;/p-1/t13-,14-,16-,18-;/m0./s1
InChIKey JALVHLYSWUUALQ-OYDMLLMWSA-M
Mol Weight 423.4 g/mol
Molecular Formula C18H34INO2
Exact Mass 423.163424 g/mol
Parent InChIKey OGGBONXCZDHPBH-DNUAJFIVSA-M
Enantiomer InChIKey JALVHLYSWUUALQ-YXCQCANPSA-M

View Spectrum of TRIMETHYL-[(+/-)-1-BETA-TERT.-BUTOXY-7A-BETA-METHYL-2,3,3A-ALPHA,6,7,7A-HEXAHYDRO-5(4H)-OXO]-1H-INDEN-6-ALPHA-YL-METHYL-AMMONIUMIODIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
#15;(+/-)-1-BETA-TERT.-BUTOXY-6-ALPHA-DIMETHYLAMINOMETHYL-7A-BETA-METHYL-2,3,3A-ALPHA,6,7,7A-HEXAHYDRO-1H-INDEN-5(4H)-ONE
(+,-)-1b-t-butoxy-6a-dimethylaminomethyl-7ab-methyl-2,3,3aa,6,7,7a-hexahydro-1H-inden-5-(4H)-one
(1S,3aS,7aS)-1-tert-butoxy-4,4,7a-trimethyl-1,2,3,3a,6,7-hexahydroinden-5-one
7-tert-Butoxy-2,2,6-trimethylbicyclo[4.3.0]nonan-3-one
5H-INDEN-5-ONE, 1-(1,1-DIMETHYLETHOXY)-4-ETHYLOCTAHYDRO-7a-METHYL-
[1S,3aS,4S,7aS]-(+)-1-tert-Butoxy-4-ethyl-7a-methyl-3a,4,7,7a-tetrahydro-5(6)-indan-5-one
2(1H)-Naphthalenone, 5-(1,1-dimethylethoxy)octahydro-4a-methyl-1-methylene-, [4aS-(4a.alpha.,5.alpha.,8a.beta.)]-
3Ab, 8a-dimethyl-3b-methoxymethoxy-1,2,3,3a,6,7,8,8a-octahydro-azulen-4(5H)-one
(1S*,6R*,7R*,10R*)-1,6-dimethyl-10-ethoxybicyclo[5.3.0]decan-2-one
(1S*,6R*,7R*,10R*)-1,6-DIMETHYL-10-ETHOXYBICYCLO-[5.3.0]-DECAN-2-OL
Title Journal or Book Year
The Structure and Function of Estrogens. XI. Synthesis of (±)-7(8→11α)abeo-Estradiol and Its 9,11-Didehydro Derivative Australian Journal of Chemistry 1992
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