5'-O-(4,4'-DIMETHOXY-TRITYL)-N6-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE
Compound with spectra: 1 NMR
![5'-O-(4,4'-DIMETHOXY-TRITYL)-N6-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE](/api/compound/5s97qIxMJtq.png?ph=true&h=300&w=458 "5'-O-(4,4'-DIMETHOXY-TRITYL)-N6-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE")
| SpectraBase Compound ID | 5s97qIxMJtq |
|---|---|
| InChI | InChI=1S/C42H55N5O7Si/c1-27(2)55(28(3)4,29(5)6)53-26-51-38-37(48)35(54-41(38)47-25-46-36-39(43-7)44-24-45-40(36)47)23-52-42(30-13-11-10-12-14-30,31-15-19-33(49-8)20-16-31)32-17-21-34(50-9)22-18-32/h10-22,24-25,27-29,35,37-38,41,48H,23,26H2,1-9H3,(H,43,44,45)/t35-,37-,38-,41?/m0/s1 |
| InChIKey | NNZQYXISTWPVCG-XSKZIOPQSA-N |
| Mol Weight | 770.0 g/mol |
| Molecular Formula | C42H55N5O7Si |
| Exact Mass | 769.387076 g/mol |
| Enantiomer InChIKey | NNZQYXISTWPVCG-DPHXJLRXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-BENZOYL-5'-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-ADENOSINE
9-(2-O-TETRAHYDROPYRANYL-BETA-L-RIBOFURANOSYL)-N(6)-BENZOYL-ADENOSINE;(DIASTEREOMER-1)
2',3'-ISOPROPYLIDENE-N6-AMINOETHYL-ADENOSINE-5'-MONOPHOSPHATE;N6-AE-AMP-AC
Adenosine, 3'-O-methyl-5'-O-(triphenylmethyl)-, 2'-acetate
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(methylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
(5R)-2-(acetoxymethyl)-5-(6-(furan-3-ylmethylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
9-(2'-DEOXY-2'-FLUORO-5'-O-TRITYL-BETA-D-ARABINOFURANOSYL)-N(6)-TRITYLADENINE
(2R,3R,4R,5R)-2-(6-((E)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
(2R,3R,4R,5R)-2-(6-((Z)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(3-methylbut-2-enylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
| Title | Journal or Book | Year |
|---|---|---|
| The Synthesis of 2?- O -[(Triisopropylsilyl)oxy] methyl ( TOM ) Phosphoramidites of Methylated Ribonucleosides ( m 1 G , m 2 G , m 2 2 G , m 1 I , m 3 U , m 4 C , m 6 A , m 6 2 A ) for Use in Automated RNA Solid-Phase Synthesis | Monatshefte f�r Chemie / Chemical Monthly | 2003 |