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EXO-4-HYDROXY-CIS-1-THIONIABICYCLO-[3.3.0]-OCTANE-IODIDE

Compound with spectra: 1 NMR

EXO-4-HYDROXY-CIS-1-THIONIABICYCLO-[3.3.0]-OCTANE-IODIDE
SpectraBase Compound ID Epm8bw8sigw
InChI InChI=1S/C7H13OS.HI/c8-6-3-5-9-4-1-2-7(6)9;/h6-8H,1-5H2;1H/q+1;/p-1/t6-,7+,9?;/m1./s1
InChIKey IDMCHPHTGFZLAN-ZUGNLDISSA-M
Mol Weight 272.14 g/mol
Molecular Formula C7H13IOS
Exact Mass 271.973181 g/mol
Parent InChIKey MNLLWVOHUOMRBE-CSTAXXSYSA-M
Enantiomer InChIKey IDMCHPHTGFZLAN-AQLFBIHGSA-M

View Spectrum of EXO-4-HYDROXY-CIS-1-THIONIABICYCLO-[3.3.0]-OCTANE-IODIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
2-(Hexylthio)cyclohexanol
1,4-Dithiabutane, 1,4-bis(1-hydroxy-2-cyclohexyl)-
L-ARABINOSE, 1-THIOOCTYL-
5-(nonylthio)pentane-1,2,3,4-tetrol
LYXITOL, 1-THIONONYL-
1-(2-Methyl-1,3-dithian-2-yl)-1-butanol
(+-)-N-[(2'R*,3'S*)-2'-Methylthio-3'-hydrohxyexyl]acetamide
(1S,2S)-3-Methylsulfanyl-cyclohex-3-ene-1,2-diol
(2S,3S)-2-(hydroxymethyl)-2-methyl-3-thianol
NYAAKHZINSYUQB-BDAKNGLRSA-N
Title Journal or Book Year
Regio- and Stereospecific Me3SiI-Promoted Intramolecular Displacement of Hydroxy Group by Sulfide. 2. Polyhydroxylated Thiepane Ring Contraction to Thiolane or Thiane Derivatives. Synthesis of Enantiopure Polyalcohols1 The Journal of Organic Chemistry 1997
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