4-[TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]-N-METHYL-TRIFLUORACETAMIDE;MAJOR-ROTAMER
Compound with spectra: 2 NMR
![4-[TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]-N-METHYL-TRIFLUORACETAMIDE;MAJOR-ROTAMER](/api/compound/2hXL8gZ8Y5k.png?ph=true&h=300&w=458 "4-[TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]-N-METHYL-TRIFLUORACETAMIDE;MAJOR-ROTAMER")
| SpectraBase Compound ID | 2hXL8gZ8Y5k |
|---|---|
| InChI | InChI=1S/2C13H24F3NO2Si/c2*1-12(2,3)20(5,6)19-10-8-7-9-17(4)11(18)13(14,15)16/h2*7-8H,9-10H2,1-6H3/b2*8-7+ |
| InChIKey | BXTKRSZOPIDKKF-ONYUMSKCSA-N |
| Mol Weight | 622.84 g/mol |
| Molecular Formula | C26H48F6N2O4Si2 |
| Exact Mass | 622.30568 g/mol |
| 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 |
- 4-[TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]-N-METHYL-TRIFLUORACETAMIDE;MINOR-ROTAMER
N-[(Z)-6-[tert-butyl(dimethyl)silyl]oxyhex-4-enyl]carbamic acid tert-butyl ester
(Z)-N-{4-[(Methoxycarbonyl)oxy]but-2-enyl}-N-(prop-2'-enyl)-trifluoroacetamide
(Z,Z)-1-t-Butyldimethylsilyloxy-4-methoxy-2,4-nonadiene
(Z)-1,5-BIS-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-PENT-3-EN-2-OL
(Z)-1,4-BIS-(1,1-DIMETHYL-1-(1,1,2-TRIMETHYLPROPYL)-SILYLOXY)-2-BUTENE
Ethyl (3E)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-fluoropent-3-enoate
Ethyl (E)-4-(tert-butyldimethylsilyloxy)-2-iodo-2-butenoate
Ethyl (E)-4-[(t-butyl)dimethylsilyloxy]-2-methylbut-2-enoate
(2E)-2-[2-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-ETHYLIDENE]-6-METHYL-HEPT-5-EN-1-OL
(2Z)-2-[2-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-ETHYLIDENE]-6-METHYL-HEPT-5-EN-1-OL
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of α-Amino-γ-lactams through Pd-Catalzed Intramolecular Allylic Alkylation of Sarcosine Allyl Amides | European Journal of Organic Chemistry | 2014 |