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

Compound with spectra: 4 NMR

(E)-1-(Tributylstannyl)-4-(methyl)-4-((trimethylsilyl)oxy)-1-octene
SpectraBase Compound ID L6l1V89rTMX
InChI InChI=1S/C12H25OSi.3C4H9.Sn/c1-7-9-11-12(3,10-8-2)13-14(4,5)6;3*1-3-4-2;/h2,8H,7,9-11H2,1,3-6H3;3*1,3-4H2,2H3;
InChIKey QPDPSYPQQVBCLH-UHFFFAOYSA-N
Mol Weight 503.5 g/mol
Molecular Formula C24H52OSiSn
Exact Mass 504.280945 g/mol

View Spectrum of (E)-1-(Tributylstannyl)-4-(methyl)-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-(methyl)-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-(methyl)-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-(methyl)-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-(methyl)-4-((trimethylsilyl)oxy)-1-octene
(E)-1-Tributylstannyl-4-phenylpenten-4-ol
(E)-1-Tributylstannyl-4-(4'-methoxyphenyl)buten-4-ol
3-Methyl-3-[(Z)-2'-(tributylstannyl)vinyl]-cyclopentan-1-one
(9S,10E)-11-(TRIBUTYLSTANNYL)-2-IODO-9-(1-METHYLETHYL)-UNDEC-1-EN-6-ONE
Terpineol <1->, mono-TMS
(1S,2E)-1-(1'-Methyl)ethyl-3-tributylstannyl-N-(t-butoxycarbonyl)-2-propenamine
4-((Tert-butyldimethylsilyl)oxy)-4-methyloctan-2-one
(E,4R)-4-methyl-2-tributylstannyl-2-octen-1-ol
(6R,2E/Z,7E)-6-(tert-Butyldimethylsilyloxy)nona-2,7-dienyl(tributyl)stanname
(E)-N-(tert-Butoxycarbonyl)-2-propenyl-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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