2'-DEOXYADENOSIN-5'-YL-H-PHOSPHONATE_TRIETHYLAMMONIUM_SALT
Compound with spectra: 1 NMR
| SpectraBase Compound ID | CXAjA3nUs7j |
|---|---|
| InChI | InChI=1S/C10H14N5O5P.C6H15N/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(20-7)2-19-21(17)18;1-4-7(5-2)6-3/h3-7,16,21H,1-2H2,(H,17,18)(H2,11,12,13);4-6H2,1-3H3/t5-,6+,7+;/m0./s1 |
| InChIKey | JAKSWSOPUTZGCR-VWZUFWLJSA-N |
| Mol Weight | 416.42 g/mol |
| Molecular Formula | C16H29N6O5P |
| Exact Mass | 416.193705 g/mol |
| Parent InChIKey | QIZHRNQOUYDQAE-RRKCRQDMSA-N |
| Enantiomer InChIKey | JAKSWSOPUTZGCR-NLRFIBDTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | H2O:NAOD;PH=8 |
2'-Deoxyadenosine 5'-monophosphate monohydrate
2'-Deoxyadenosine-5'-monophosphate
2'-DEOXYANDENOSINE 5'-PHOSPHATE, DISODIUM SALT, MONOHYDRATE
acrylic acid [(2R,3S,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
5'-O-CARBAZOYL-2'-DEOXYADENOSINE
butyric acid [(2R,3S,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
2-chloroacetic acid [(2R,3S,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
Adenosine, 2'-deoxy-3'-O-methyl-
(2R,3S,5R)-5-(6-methylaminopurin-9-yl)-2-methylol-tetrahydrofuran-3-ol
N6-Methyl-2'-deoxy-adenosine
| Title | Journal or Book | Year |
|---|---|---|
| Nucleoside H-Phosphonates. 18. Synthesis of Unprotected Nucleoside 5‘-H-Phosphonates and Nucleoside 5‘-H-Phosphonothioates and Their Conversion into the 5‘-Phosphorothioate and 5‘-Phosphorodithioate Monoesters | The Journal of Organic Chemistry | 1998 |
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.