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N-{(1S,2R)-2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-METHYLPROPYL}-ACETAMIDE

Compound with spectra: 1 NMR, and 1 MS (GC)

N-{(1S,2R)-2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-METHYLPROPYL}-ACETAMIDE
SpectraBase Compound ID 31itpzPQpHi
InChI InChI=1S/C12H27NO2Si/c1-9(13-11(3)14)10(2)15-16(7,8)12(4,5)6/h9-10H,1-8H3,(H,13,14)/t9-,10+/m0/s1
InChIKey RICQUCHVGXUHDF-VHSXEESVSA-N
Mol Weight 245.44 g/mol
Molecular Formula C12H27NO2Si
Exact Mass 245.181106 g/mol
Enantiomer InChIKey RICQUCHVGXUHDF-ZJUUUORDSA-N

View Spectrum of N-{(1S,2R)-2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-METHYLPROPYL}-ACETAMIDE

MS (GC) Spectrum
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Source of Spectrum H-72-422-21

View Spectrum of N-{(1S,2R)-2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-METHYLPROPYL}-ACETAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Acetamide, N-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-methylpropyl]-, [R-(R*,S*)]-
N-[2-[tert-butyl(dimethyl)silyl]oxy-1-methyl-propyl]acetamide
2-Methylbutanoic acid, 3-(t-butyldimethylsilyloxy)-
(2R)-2-[(tert-butyl)dimethylsilyloxy]-3-methyloctane
tert-Butyl-dimethyl-(2-piperidinylmethoxy)silane
(4R,5S,E)-5-(tert-Butyldimethylsilyloxy)-4-hydroxyhex-2-enal
(2R,3S)-2-tert-Butyldimethylsiloxy-3-methylpent-4-enenitrile
(2R,4S)-4-{[(t-Butyldimethyl)silyloxy]methyl}azetidine-2-methanol
(2R,3R)-3-[tert-butyl(dimethyl)silyl]oxy-2,4-dimethyl-valeraldehyde
(2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-methyl-pent-4-enal
5S-(tert-Butyldimethylsilyloxy)hexanoic acid methoxymethylamide
Title Journal or Book Year
Elektrochemische Decarboxylierung vonL.-Threonin- und Oligopeptid-Derivaten unter Bildung vonN-Acyl-N, O-acetalen: Herstellung von Oligopeptiden mit Carboxamid-oder Phosphonat-C-Terminus Helvetica Chimica Acta 1989
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