METHYL-N-{2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-CYANOPROPYL}-CARBAMATE
Compound with spectra: 2 NMR
![METHYL-N-{2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-CYANOPROPYL}-CARBAMATE](/api/compound/UXWFNvK24u.png?ph=true&h=300&w=458 "METHYL-N-{2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-CYANOPROPYL}-CARBAMATE")
| SpectraBase Compound ID | UXWFNvK24u |
|---|---|
| InChI | InChI=1S/C12H24N2O3Si/c1-9(10(8-13)14-11(15)16-5)17-18(6,7)12(2,3)4/h9-10H,1-7H3,(H,14,15)/t9-,10-/m1/s1 |
| InChIKey | OTCUILBSDPEXBA-NXEZZACHSA-N |
| Mol Weight | 272.42 g/mol |
| Molecular Formula | C12H24N2O3Si |
| Exact Mass | 272.155619 g/mol |
| Enantiomer InChIKey | OTCUILBSDPEXBA-UWVGGRQHSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- METHYL-N-{(1R,2R)-2-{[(TERT.-BUTYL)-DIMETHYLSILYL]-OXY}-1-CYANOPROPYL}-CARBAMATE
4-[(t-Butyl)dimethylsilyl]oxy-5-methyl-2-pyrrolidinone
Methyl allyl(2-([tert-butyl(dimethyl)silyl]oxy)propyl)carbamate
(t-butyl)dimethylsilyl N-isobutyloxycarbonyl-.alpha.-aminopropanoate
BENZYL-(S)-[1-(TERT.-BUTYLDIMETHYLSILANYLOXYMETHYL)-ALLYL]-CARBAMATE
(phenylmethyl) N-[(2S)-1-[tert-butyl(dimethyl)silyl]oxy-3-oxidanyl-propan-2-yl]carbamate
(2S,3S)-1-tert-Butyldimethylsilyloxy-3-tert-butoxycarbonylamino-2-butanol
(2S,4R)-4-[[1-(TERT.-BUTYL)-1,1-DIMETHYLSILYL]-OXY]-2-METHOXYMETHYL-PYRROLIDIN
Methyl (3S,1'S)-3-[1-(1,1-dimethylethyldimethylsiloxy)ethyl]-4-pentenedithioate
(S)-(+)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one oxime
(+/-)-(3S,4S)-3,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-3,4-DIHYDROXY-PYRROLIDINE
| 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 |