1,1,2,3,4,5-HEXA-O-ACETYL-ALDEHYDO-L-RIBOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Ad1agGY0SWo |
|---|---|
| InChI | InChI=1S/C17H24O12/c1-8(18)24-7-14(25-9(2)19)15(26-10(3)20)16(27-11(4)21)17(28-12(5)22)29-13(6)23/h14-17H,7H2,1-6H3/t14-,15-,16-/m0/s1 |
| InChIKey | PCWVNHHXSDHRDP-JYJNAYRXSA-N |
| Mol Weight | 420.37 g/mol |
| Molecular Formula | C17H24O12 |
| Exact Mass | 420.126776 g/mol |
| Enantiomer InChIKey | PCWVNHHXSDHRDP-BZUAXINKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1,2,3,4,5,6,7-Hepta-O-acetylheptitol
Glucitol, 6-deoxy-6-fluoro-, pentaacetate, D-
2,3,4,5,6-PENTA-O-ACETYL-1-DEOXY-1-AMINO-D-GLUCITOL-HYDROBROMIDE
1,2,3,4,5-PENTA-O-ACETYL-6,7,8-TRIDEOXY-L-GALACTO-7-OCTENITOL
1,3,4,5-tetra-O-acetyl-1-deuterio-2-O-methyl-L-arabinitol
1,3,4-tri-O-Acetyl.beta.,L-arabinopyranose
PMAA of 1,4,5-Triacetyl-6-(methoxyethyl)-2,3-dimethylglucitol from 1,4-linked glucose
4,5,6-Tri-O-acetyl-2,3-di-O-methyl-D-mannonitrile
PMAA of 1,4,5-Triacetyl-2-(methoxyethyl)-3,6-dimethylglucitol from 1,4-linked glucose
3,4,5-Tri-O-acetyl-2,6-di-O-methyl-D-mannonitrile
| Title | Journal or Book | Year |
|---|---|---|
| Reaction Kinetics and Mechanism of Sulfuric Acid-Catalyzed Acetolysis of Acylated Methyl L-Ribofuranosides | European Journal of Organic Chemistry | 2009 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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