2',3'-O-ISOPROPYLIDENE-5'-O-[6-[(TOL-4-YL)-SULFONYLOXY]-HEXYL]-ADENOSINE
Compound with spectra: 1 NMR
![2',3'-O-ISOPROPYLIDENE-5'-O-[6-[(TOL-4-YL)-SULFONYLOXY]-HEXYL]-ADENOSINE](/api/compound/IcykF7BSz6r.png?ph=true&h=300&w=458 "2',3'-O-ISOPROPYLIDENE-5'-O-[6-[(TOL-4-YL)-SULFONYLOXY]-HEXYL]-ADENOSINE")
| SpectraBase Compound ID | IcykF7BSz6r |
|---|---|
| InChI | InChI=1S/C26H35N5O7S/c1-17-8-10-18(11-9-17)39(32,33)35-13-7-5-4-6-12-34-14-19-21-22(38-26(2,3)37-21)25(36-19)31-16-30-20-23(27)28-15-29-24(20)31/h8-11,15-16,19,21-22,25H,4-7,12-14H2,1-3H3,(H2,27,28,29)/t19-,21-,22-,25-/m0/s1 |
| InChIKey | BGCBIERVMQMEHZ-RHQSAMMMSA-N |
| Mol Weight | 561.7 g/mol |
| Molecular Formula | C26H35N5O7S |
| Exact Mass | 561.22572 g/mol |
| Enantiomer InChIKey | BGCBIERVMQMEHZ-PTGPVQHPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2',3'-O-ISOPROPYLIDENE-5'-O-[7-[(TOL-4-YL)-SULFONYLOXY]-HEPTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[4-[(TOL-4-YL)-SULFONYLOXY]-BUTYL]-ADENOSINE
5'-O-(6-HYDROXYETHYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(7-HYDROXYHEPTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
5'-O-(5-HYDROXYPENTYL)-2',3'-ISOPROPYLIDENE-ADENOSINE
5'-O-(4-HYDROXYBUTYL)-2',3'-O-ISOPROPYLIDENE-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[7-(TETRAHYDRO-2H-PYRAN-2-YL)-HEPTYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[6-(TETRAHYDRO-2-H-PYRAN-2-YL)-HEXYL]-ADENOSINE
2',3'-O-ISOPROPYLIDENE-5'-O-[5-(TETRAHYDRO-2H-PYRAN-2-YL)-PENTYL]-ADENOSINE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and Characterization of (5′-Deoxyadenosin-5′-yl)cobalamin ( = ‘Adenosylcobalamin’) Analogues Mimicking the Transition-State Geometry of Coenzyme-B12-Dependent Rearrangements | Helvetica Chimica Acta | 1993 |