4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin
Compound with spectra: 1 NMR
![4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin](/api/compound/I0ipDCuX2Uq.png?ph=true&h=300&w=458 "4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin")
| SpectraBase Compound ID | I0ipDCuX2Uq |
|---|---|
| InChI | InChI=1S/C21H20N5O9P/c1-30-11-2-3-13-12(5-11)10(4-15(27)33-13)6-31-36(29)32-7-14-18(35-36)17(28)21(34-14)26-9-25-16-19(22)23-8-24-20(16)26/h2-5,8-9,14,17-18,21,28H,6-7H2,1H3,(H2,22,23,24)/t14-,17-,18-,21-,36-/m1/s1 |
| InChIKey | QUYVRKGPKPPWQC-ATDUASFFSA-N |
| Mol Weight | 517.39 g/mol |
| Molecular Formula | C21H20N5O9P |
| Exact Mass | 517.099864 g/mol |
| Enantiomer InChIKey | QUYVRKGPKPPWQC-HRCHOMNGSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
4-[[(1S,3S,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-7-dimethylamino-coumarin
4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-7-dimethylamino-coumarin
VILPZALHFBLWBO-ONMZBTRXSA-N
Adenosine-3',5'-cyclic-[S-(p)]-[4-[N,N-bis-(2-(trimethylsilyl)-ethoxycarbonylmethyl)-carbamoyl]-2-nitrophenyl]-methyl-phosphonate
ADENOSINE-3',5'-CYCLIC-[R-(P)]-[4-[N,N-BIS-(2-(TRIMETHYLSILYL)-ETHOXYCARBONYLMETHYL)-CARBAMOYL]-2-NITROPHENYL]-METHYL-PHOSPHONATE
2'-O-TERT.-BUTYL-DIMETHYLSILYL-5'-O-PARA-METHOXYTRITYL-ADENOSINE-DIETHYL-3'-PHOSPHATE
(S-p)-Uridylyl-(3'->5')-N(1)-methyladenosine-methylester
(R-p)-[17-o,18-o]-Uridylyl-3'->5'-adenosine
5'-o-(Uridin-3'-yloxythiophosphoryl)adenosine (diastereomer mixture)
| Title | Journal or Book | Year |
|---|---|---|
| Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 2. Photocleavage of Selected (Coumarin-4-yl)methyl-Caged Adenosine Cyclic 3‘,5‘-Monophosphates with Fluorescence Enhancement | The Journal of Organic Chemistry | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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