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

Compound with spectra: 4 NMR

(E)-1-(Tributylstannyl)-4-(difluoromethyl)-4-((trimethylsilyl)oxy)-1-octene
SpectraBase Compound ID CKQ9TjEqWhZ
InChI InChI=1S/C12H23F2OSi.3C4H9.Sn/c1-6-8-10-12(9-7-2,11(13)14)15-16(3,4)5;3*1-3-4-2;/h2,7,11H,6,8-10H2,1,3-5H3;3*1,3-4H2,2H3;
InChIKey QNDXEPPHMUXGDC-UHFFFAOYSA-N
Mol Weight 539.5 g/mol
Molecular Formula C24H50F2OSiSn
Exact Mass 540.262101 g/mol

View Spectrum of (E)-1-(Tributylstannyl)-4-(difluoromethyl)-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-(difluoromethyl)-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-(difluoromethyl)-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-(difluoromethyl)-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-(difluoromethyl)-4-((trimethylsilyl)oxy)-1-octene
(E)-TRIBUTYL(4-TRIMETHYLSILYLOXY-4-METHYL-5-PHENOXYPENT-1-ENYL)STANNANE
(1E,3R*,4R*)-3-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-1-(TRIBUTYLSTANNYL)-HEX-1-ENE-4-OL;SYN-ISOMER
(4S,6R,10E)-1-(BENZYLOXY)-4,6-O-ISOPROPYLIDENE-11-(TRIBUTYLSTANNYL)-10-UNDECENE-4,6-DIOL
6-Undecen-5-ol, 6-(tributylstannyl)-, (E)-
(Z)-2-p-Cyclohexenyl-1-tributylstannyl-1,4-pentadiene
Tributyl-[(E)-(2-isopropyl-3-piperidylidene)methyl]stannane
(1S,2E)-1-Benzyl-3-tributylstannyl-N-(t-butoxycarbonyl)-2-propenamine
(2R,3R,Z)-3-((4-Methoxybenzyl)oxy)-2-methyl-5-(tributylstannyl)pent-4-en-1-ol
2-[2'-Tributylstannylethenyl]acetanilide
(Z)-N-(tert-Butoxycarbonyl)-2-methoxycarbonyl-3-tributylstannyl-2-propen-1-amine
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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