#7A;TERT.-BUTYL-N-[3-[2-[2-[3-[[4-[(1R,2R)-2-HYDROXY-1-(HYDROXYMETHYL)-PROPYL]-AMINO]-4-OXO-BUTANOYL]-AMINO]-PROPOXY]-ETHOXY]-ETHOXY]-PROPYL]-CARBAMATE
Compound with spectra: 1 NMR
![#7A;TERT.-BUTYL-N-[3-[2-[2-[3-[[4-[(1R,2R)-2-HYDROXY-1-(HYDROXYMETHYL)-PROPYL]-AMINO]-4-OXO-BUTANOYL]-AMINO]-PROPOXY]-ETHOXY]-ETHOXY]-PROPYL]-CARBAMATE](/api/compound/8FtXLeJsmvo.png?ph=true&h=300&w=458 "#7A;TERT.-BUTYL-N-[3-[2-[2-[3-[[4-[(1R,2R)-2-HYDROXY-1-(HYDROXYMETHYL)-PROPYL]-AMINO]-4-OXO-BUTANOYL]-AMINO]-PROPOXY]-ETHOXY]-ETHOXY]-PROPYL]-CARBAMATE")
| SpectraBase Compound ID | 8FtXLeJsmvo |
|---|---|
| InChI | InChI=1S/2C23H45N3O9/c2*1-18(28)19(17-27)26-21(30)8-7-20(29)24-9-5-11-32-13-15-34-16-14-33-12-6-10-25-22(31)35-23(2,3)4/h2*18-19,27-28H,5-17H2,1-4H3,(H,24,29)(H,25,31)(H,26,30)/t2*18-,19-/m11/s1 |
| InChIKey | UQAYVONNRDTJLY-OIZIJXTKSA-N |
| Mol Weight | 1015.3 g/mol |
| Molecular Formula | C46H90N6O18 |
| Exact Mass | 1014.63116 g/mol |
| Enantiomer InChIKey | UQAYVONNRDTJLY-BYPDJTGLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
8-[4-(DITHIOLAN-3-YL)-BUTANOYLAMINO]-N-[(1R,2R)-2-HYDROXY-1-(HYDROXYMETHYL)-PROPYL]-OCTAN-AMIDE
1,3-DIHYDROXY-2-HEXANOYLAMINO-4E-HEPTADECENE
D-ERYTHRO-SPHINGANINE
(2S,3R)-2-(DOCOSANOYLAMINO)-NONADECANE-1,3-DIOL
N-[(2S,3R,4E)-1,3-DIHYDROXY-15-METHYLHEXADEC-4-EN-2-YL]-21-METHYLDOCOSANAMIDE
N-t-Butoxycarbonyl-D-erythro-dihydrosphingosine
6-AZIDO-N-[BIS-(N'-TERT.-BUTOXYCARBONYLAMINOMETHYL)-METHYL]-HEXANAMIDE
N-[(7-keto-1,4-diazepan-5-yl)methyl]carbamic acid tert-butyl ester
Methyl 4-{(1R,2R)-N-[(2-hydroxycyclohexyl)carbamoyl]}butyrate
N-[BIS-(N'-TERT.-BUTOXYCARBONYLAMINOMETHYL)-METHYL]-6-ISOTHIOCYANATOHEXANAMIDE
| Title | Journal or Book | Year |
|---|---|---|
| Thioctic Acid Derivatives as Building Blocks to Incorporate DNA Oligonucleotides onto Gold Nanoparticles | Molecules | 2014 |