5'-O-(4,4'-DIMETHOXY-TRITYL)-N2-METHYL-O6-[2-(4-NITROPHENYL)-ETHYL]-GUANOSINE
Compound with spectra: 1 NMR
![5'-O-(4,4'-DIMETHOXY-TRITYL)-N2-METHYL-O6-[2-(4-NITROPHENYL)-ETHYL]-GUANOSINE](/api/compound/65u1A1ze5sY.png?ph=true&h=300&w=458 "5'-O-(4,4'-DIMETHOXY-TRITYL)-N2-METHYL-O6-[2-(4-NITROPHENYL)-ETHYL]-GUANOSINE")
| SpectraBase Compound ID | 65u1A1ze5sY |
|---|---|
| InChI | InChI=1S/C40H40N6O9/c1-41-39-43-36-33(37(44-39)53-22-21-25-9-15-29(16-10-25)46(49)50)42-24-45(36)38-35(48)34(47)32(55-38)23-54-40(26-7-5-4-6-8-26,27-11-17-30(51-2)18-12-27)28-13-19-31(52-3)20-14-28/h4-20,24,32,34-35,38,47-48H,21-23H2,1-3H3,(H,41,43,44)/t32-,34-,35-,38-/m0/s1 |
| InChIKey | KGHSXHZMTSXACR-SQUJSISRSA-N |
| Mol Weight | 748.8 g/mol |
| Molecular Formula | C40H40N6O9 |
| Exact Mass | 748.285677 g/mol |
| Enantiomer InChIKey | KGHSXHZMTSXACR-NFXQKKKASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
FMZJIQCFGXZGBW-IQZMFCRQSA-N
QMYFTEOOGMIZJZ-CDSYHYPYSA-N
LVQXPKTVEGRRFW-CDSYHYPYSA-N
NGPCISHQTVWIHK-CDSYHYPYSA-N
PKDHQIUQVXSINZ-JLPWOHBFSA-N
N2-ACETYL-6-CHLORO-9-[3',5'-DI-O-ACETYL-2'-O-(2-TRIFLUOROACETAMIDO)-ETHYL-BETA-D-RIBOFURANOSYL]-PURINE
P1-5'-O-ADENOSINE-P3-5'-O-URIDINE-TRIPHOSPHATE-SODIUM-SALT
ADENOSINE-5'-PHOSPHORO-AMINOBENZIMIDAZOLIDE
(2R,3R,4S,5R)-2-(2-amino-6-ethoxy-8-methylsulfanyl-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
[(3aR,4R,6R,6aR)-4-(2-amino-6-methoxy-purin-9-yl)-2-oxo-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3,2]dioxathiol-6-yl]methyl acetate
| 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 |