N-(6)-(4-TOLYLSULFONYLETHYL)_ADENOSINE;A-N6-TSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 9w0fjjYDG3V |
|---|---|
| InChI | InChI=1S/C19H23N5O6S/c1-11-2-4-12(5-3-11)31(28,29)7-6-20-17-14-18(22-9-21-17)24(10-23-14)19-16(27)15(26)13(8-25)30-19/h2-5,9-10,13,15-16,19,25-27H,6-8H2,1H3,(H,20,21,22)/t13-,15-,16-,19-/m0/s1 |
| InChIKey | FVVCDWBIICEKKD-FJXLLPKBSA-N |
| Mol Weight | 449.48 g/mol |
| Molecular Formula | C19H23N5O6S |
| Exact Mass | 449.136905 g/mol |
| Enantiomer InChIKey | FVVCDWBIICEKKD-NVQRDWNXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:CD3OD |
N6-(4-METHOXYBENZYL)-ADENOSINE
N-(6)-(4-HYDROXYBENZYL)-ADENINE_RIBOSIDE
N6-(3-HYDROXYBENZYL)-ADENOSINE
Kinetin riboside
Adenosine, N-(2-furanylmethyl)-
Adenosine, N-(2,3-dihydroxy-3-methylbutyl)-
N6-(2-HYDROXYBENZYL)-ADENOSINE
N6-(2-CHLOROBENZYL)-ADENOSINE
N6-(2-METHOXYBENZYL)-ADENOSINE
SQMWSBKSHWARHU-OXUWNYNTSA-N
| Title | Journal or Book | Year |
|---|---|---|
| High-quality oligo-RNA synthesis using the new 2′-O-TEM protecting group by selectively quenching the addition of p-tolyl vinyl sulphone to exocyclic amino functions | Canadian Journal of Chemistry | 2007 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.