5'-O-(4,4'-DIMETHOXY-TRITYL)-N6,N6-DI-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE
Compound with spectra: 1 NMR
![5'-O-(4,4'-DIMETHOXY-TRITYL)-N6,N6-DI-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE](/api/compound/9JrdvBfBWFe.png?ph=true&h=300&w=458 "5'-O-(4,4'-DIMETHOXY-TRITYL)-N6,N6-DI-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE")
| SpectraBase Compound ID | 9JrdvBfBWFe |
|---|---|
| InChI | InChI=1S/C43H57N5O7Si/c1-28(2)56(29(3)4,30(5)6)54-27-52-39-38(49)36(55-42(39)48-26-46-37-40(47(7)8)44-25-45-41(37)48)24-53-43(31-14-12-11-13-15-31,32-16-20-34(50-9)21-17-32)33-18-22-35(51-10)23-19-33/h11-23,25-26,28-30,36,38-39,42,49H,24,27H2,1-10H3/t36-,38-,39-,42-/m0/s1 |
| InChIKey | IHLBCXHTKVMNCL-ZBWBOEHLSA-N |
| Mol Weight | 784.0 g/mol |
| Molecular Formula | C43H57N5O7Si |
| Exact Mass | 783.402726 g/mol |
| Enantiomer InChIKey | IHLBCXHTKVMNCL-CISTVLBBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5'-O-(4,4'-DIMETHOXY-TRITYL)-N6-METHYL-2'-O-[[(TRI-ISOPROPYL-SILYL)-OXY]-METHYL]-ADENOSINE
(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-[tert-butyl(dimethyl)silyl]oxy-2-[[(4-methoxyphenyl)-diphenyl-methoxy]methyl]oxolan-3-ol
N-BENZOYL-5'-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-ADENOSINE
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(dimethylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
Benzamide, N-[9-[3-O-benzoyl-5-O-[(4-methoxyphenyl)diphenylmethyl]-.beta.-D-xylo furanosyl]-9H-purin-6-yl]-
2',3'-O-isopropylidene-N(6)-methyl-N(6)-formyl-adenosine
Adenosine, 3'-O-methyl-5'-O-(triphenylmethyl)-, 2'-acetate
N(6),n(6),o-2',3',5'-penta(methyl-D3)adenosine
9-(2-O-TETRAHYDROPYRANYL-BETA-L-RIBOFURANOSYL)-N(6)-BENZOYL-ADENOSINE;(DIASTEREOMER-1)
N2-ACETYL-9-[5'-O-(4,4'-DIMETHOXYTRITYL)-2'-O-(2-TRIFLUOROACETAMIDO)-ETHYL-BETA-D-RIBOFURANOSYL]-PURINE
| 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 |