(1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-6-azido-4-hydroxy-cyclohexane-1,2,3-triyl Triacetate
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | HvvmNd6sVxZ |
|---|---|
| InChI | InChI=1S/C15H21N3O9/c1-7(19)24-6-15(23)5-11(17-18-16)12(25-8(2)20)13(26-9(3)21)14(15)27-10(4)22/h11-14,23H,5-6H2,1-4H3/t11-,12-,13+,14-,15-/m0/s1 |
| InChIKey | YRZMAPUDHCJEMG-RMEBNNNOSA-N |
| Mol Weight | 387.35 g/mol |
| Molecular Formula | C15H21N3O9 |
| Exact Mass | 387.127779 g/mol |
| Enantiomer InChIKey | YRZMAPUDHCJEMG-UXXRCYHCSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | U1-2014-3628-9 |
| 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 |
- (1S,2S,3R,4S,5S)-5-ACETOXYMETHYL-1-AZIDO-5-HYDROXY-2,3,4-TRI-ACETOXYCYCLOHEXANE
(1R,2S,3R,4S,5S)-1-Azido-4,5-di-O-acetyl-3-O-benzyl-5-((benzyloxy)methyl)cyclohexane-2,3,4,5-tetrol
(1S,2R,3R,4S,5S)-1-Azido-4,5-Di-O-acetyl-3-O-benzyl-5-((benzyloxy)methyl)cyclohexane-2,3,4,5-tetrol
UUBUVPXXGXNJSE-MHTWJZCWSA-N
(1R,2S,3S,4R,5R)-3-O-Acetyl-5-benzoyloxymethyl-4,5-O-cyclohexylidene-1,2,3,4,5-cyclohexanpentanol
[(3AS,5R,6S,7R,7AS)-7-(BENZOYLOXY)-5,6-DIHYDROXY-2-OXOHEXAHYDROBENZO-[D]-[1,3]-DIOXOL-3A-YL]-METHYL-BENZOATE
(+/-)-4beta-(Acetoxymethyl)-1beta-(5-amino-6-chloro-4-pyrimidinylamino)-2alpha,3alpha-O-isopropylidene-2alpha,3alpha,4alpha-cyclopentanetriol
(1R,3R,4S)-P-Menthan-3-yl O-B-D-glucopyranosyl-(1->4)-B-D-glucopyranoside heptaacetate
4-O-TERT.-BUTYLDIMETHYLSILYL-2-DEOXY-3-AZIDO-1-N-(BENZYLOXYCARBONYL)-5,6-DI-O-ACETYLSTREPTAMINE
DIGLUCOPYRANOSYLCURCUMIN-OCTAACETATE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of 1,2,3-Triazoles from Azide-Derivatised Aminocyclitols by Catalytic Diazo Transfer and CuAAC Click Chemistry | European Journal of Organic Chemistry | 2014 |
| Total Syntheses of (+)-Valiolamine and (-)-1-epi-Valiolamine from Naturally Abundant (-)-Shikimic Acid | European Journal of Organic Chemistry | 2013 |
Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library. Learn more.