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(E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene

Compound with spectra: 4 NMR

(E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene
SpectraBase Compound ID 5hJFsqMp6qZ
InChI InChI=1S/C12H24FOSi.3C4H9.Sn/c1-6-8-10-12(11-13,9-7-2)14-15(3,4)5;3*1-3-4-2;/h2,7H,6,8-11H2,1,3-5H3;3*1,3-4H2,2H3;
InChIKey UBYXOHZFTNFXBE-UHFFFAOYSA-N
Mol Weight 521.5 g/mol
Molecular Formula C24H51FOSiSn
Exact Mass 522.271523 g/mol

View Spectrum of (E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of (E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of (E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene

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

View Spectrum of (E)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (Z)-1-(Tributylstannyl)-4-(fluoromethyl)-4-((trimethylsilyl)oxy)-1-octene
(E)-1-(Tributylstannyl)-4-(chloromethyl)-4-((trimethylsilyl)oxy)-1-octene
tert-Butyl-dimethyl-[(E)-1-tributylstannyloct-1-en-3-yl]oxy-silane
(E)-TRIBUTYL[3-TRIMETHYLSILYLOXY-4-(4-FLUOROPHENOXY)BUT-1-ENYL]STANNANE
(E)-TRIBUTYL[3-TRIMETHYLSILYLOXY-4-(4-CHLOROPHENOXY)BUT-1-ENYL]STANNANE
[4-Tributylstannyl-3-butenyl] 4-methoxybenzenesulfonate
Terpineol <4->, mono-TMS
6-Undecen-5-ol, 7-(tributylstannyl)-, (E)-
1-(1'-((Trimethylsilyl)oxy)cycloheptyl)-2-buten-1-one
2-CYCLOHEXEN-1-TRIFLUOROMETHYL-1-TRIMETHYLSILYLETHER
1-(1'-((Trimethylsilyl)oxy)cyclohexyl)-2-methyl-2-propen-1-one
Title Journal or Book Year
Prostaglandins and congeners. 27. Synthesis of biologically active 16-halomethyl derivatives of 15-deoxy-16-hydroxyprostaglandin E2 The Journal of Organic Chemistry 1980
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